WO2023180701A1

WO2023180701A1 - A catheter assembly

Info

Publication number: WO2023180701A1
Application number: PCT/GB2023/050670
Authority: WO
Inventors: Oliver PFLEGER
Original assignee: Convatec Limited
Priority date: 2022-03-21
Filing date: 2023-03-20
Publication date: 2023-09-28

Abstract

A packaged catheter assembly comprising a catheter, a fluid reservoir comprising wetting fluid, and a pouch, wherein: the pouch is divided into first and second compartments; the fluid reservoir and at least a portion of the catheter are arranged in the first compartment; and a fluid collection bag is connected to the catheter and is arranged in the second compartment; and the fluid reservoir is configured to release the wetting fluid into the first compartment to wet the catheter. The pouch may comprise an interaction region operable by a user to form an opening in the pouch allowing access to at least the second compartment.

Description

A catheter assembly

Technical Field of the Invention

The present invention relates to catheter assemblies. In particular, the invention concerns packaged urinary catheter assemblies, and most particularly, but not exclusively packaged intermittent male urinary catheter assemblies, especially “closed” catheter assemblies.

Background to the Invention

Many people suffer from urinary problems that can make it difficult to pass urine. Intermittent catheter assemblies can provide a convenient and portable solution to this problem as a user is able to self-catheterise to relieve themselves as required. This reduces the effect of their urinary condition on their life and allows thm to enjoy a relatively normal lifestyle.

Before the catheter has been used, it is important that it can be easily handled and manipulated while remaining sterile. Existing catheter’s can feature a sleeve which encloses the catheter and allows it to be handled indirectly via the sleeve. However, the sleeve may itself be difficult to handle and could become slippery due to contact with wetting fluid intended to activate the surface of the catheter prior to use. This can make it difficult for the user to use the catheter, especially if they have reduced dexterity.

To allow self-catheterisation as required, closed catheter assemblies collect and retain urine using a fluid collection bag, which removes the need for urine to pass directly into a toilet. To provide a fluid collection bag that is discreet prior to use but also able to store a suitable volume of liquid, fluid collection bags can be substantially 2D prior to use, consisting of two panels joined at their periphery. However, this can cause problems for the user as they must support or hold the fluid collection bag to ensure that it fills during use.

In closed catheter assemblies, fluid collection bags are designed to collect a sufficient amount of liquid such that during use the bag does not overflow. Users can have issues when liquid does not efficiently flow within the bag, for example because the bag has been folded and compacted for a long period of time prior to use, therefore leading to an uncontrolled flow of liquid into the bag. If the liquid entering the bag does not efficiently flow within the bag, the liquid can fail to fill the total available volume of the bag. In such cases, the volume of liquid in the bag is considerably less than the bag is capable of holding, therefore leading to the bag overflowing with liquid during use which can be embarrassing for the user. Moreover, when partially filled, fluid can slosh around inside existing fluid collection bags, making them somewhat difficult to handle.

Once used, a fluid collection bag is heavy and bulky as it is filled with liquid. To allow the bag to be carried and disposed of more discretely and easily, existing bags may be provided with a drain to allow them to be emptied into a toilet. However, existing drains can either leak or are difficult to open which potentially results in inadvertent or uncontrolled release of liquid from the bag. In addition, after use the bag may be stored before cleaning or disposal, however, the drain can make storage of the bag difficult and unhygienic.

After use, the catheter can also cause problems for the user as it is dirty having just been inside the body and an inconvenient shape to be packaged/stowed discreetly as it is long and thin and resiliently biased into a straight configuration. This can mean that the user must carry additional bags or other equipment to store the catheter after use if it is not possible for them to dispose of it immediately. Where the catheter is attached to a fluid collection bag, any storage bags must also be able to contain the fluid collection bag which may also be full of liquid. This further increases the challenges of storing a used catheter assembly until disposal is possible.

Many existing packaged closed catheter assemblies contain a fluid reservoir or sachet together with a fluid collection bag and catheter. Prior to use, the fluid reservoir or sachet is burst to release wetting fluid to activate the catheter surface and render it lubricious. In releasing the wetting fluid, the fluid collection bag may also become wet, which makes handling and re-packaging of the bag difficult, in particular for users with limited dexterity. In addition, if a significant portion of wetting fluid contacts, and gets stuck to the fluid collection bag, there may not be sufficient wetting fluid to activate the whole catheter surface. As such, the lack of sufficient lubrication of the catheter surface can lead to discomfort and injury during use. When using a catheter, it is important that the catheter remains clean but when packaged this can be challenging as the catheter must be removed from the packaging. This can lead to the user touching a part of the catheter that is intended to be introduced into the body, such as the tube by accident while they attempt to remove the catheter from the packaging which can lead to a risk of infection during use. It is therefore desirable to provide packaging which is convenient and easy for the user to open and which presents the catheter to the user such that it can be removed from the packaging for use without accidentally touching a part of the catheter that should remain clean directly.

It is an object of embodiments of th present invention to at least partially overcome or alleviate the above problems and/or to provide an improved catheter assembly.

Summary of the Invention

In broad terms, the present invention concerns a catheter assembly comprising a catheter. In addition, the present invention also concerns a packaged catheter assembly comprising a pouch and the catheter assembly, wherein the pouch is configured to contain the catheter assembly within it. The pouch may be configured to contain within it any one or more of: a catheter; a fluid reservoir; a fluid collection bag; and a sleeve, any of which may be as defined in the statements of invention below.

According to a broad aspect of the present invention, there is provided a fluid collection bag for a catheter assembly, wherein the fluid collection bag comprises a cavity and the cavity is provided with a plurality of internal baffles.

The fluid collection bag may be provided in in a packaged catheter assembly, the packaged catheter assembly may comprising a pouch, a catheter, and the fluid collection bag. The packaged catheter may comprise a fluid reservoir. The fluid collection bag may be configured to receive fluid from the catheter. The catheter, fluid reservoir and fluid collection bag may be arranged within the pouch. The fluid collection bag may comprise a front panel and a rear panel. A bond between the two panels may define the (internal) cavity. The fluid collection bag of the broad aspect of the invention may comprise any of the features, including any optional features, as described in relation to the first aspect, or any other aspect, of the invention below.

According to a first aspect of the present invention there is provided a packaged catheter assembly comprising a pouch, a catheter, a fluid reservoir, and a fluid collection bag configured to receive fluid from the catheter, wherein: the catheter, fluid reservoir and fluid collection bag are arranged within the pouch; and the fluid collection bag comprises a front panel and a rear panel, and a bond between the two panels defining an internal cavity; wherein the cavity is provided with a plurality of internal baffles.

Advantageously the provision of internal baffles in the cavity means that when the cavity is partially full, the contents are restricted from sloshing around within the cavity. Notably, it is normal for the cavity to be only filled partially, as fluid collection bags are typically over-engineered to be sure to retain the contents of a full, large, bladder, but are used by individuals with all sorts of sizes of bladders and frequently used before the bladder is full.

Moreover, the baffles may provide for a controlled flow of liquid in the fluid collection bag, which can improve the flow of liquid through the internal cavity of the bag. The flow of liquid is directed to the bottom of the fluid collection bag which facilitates the ingress of liquid into and within the bag. As such, the liquid fills all of the available space in the internal cavity of the bag, therefore, reducing the risk of the bag overflowing with liquid during use. Thus, the risk of embarrassment to the user is alleviated.

The fluid collection bag may be tightly folded to enable it to fit inside the pouch to provide a compact and discrete assembly. Disadvantageously, in the prior art, the resultant fold lines may not allow the required flow of liquid within the bag despite the bag being unfolded by the user prior to use. In this situation, the provision of a fluid collection bag comprising an internal cavity provided with a plurality of internal baffles is advantageous. The internal baffles prevent the fold lines becoming too compacted before use, while still allowing the fluid collection bag to be folded to enable it to fit inside the pouch, therefore, facilitating the infill of liquid. It will be understood that the packaged catheter assembly is a closed catheter assembly, as the fluid collection bag is configured to receive fluid from the catheter. The fluid collection bag may be coupled to the catheter. The fluid collection bag may be coupled with a water-tight coupling, for example it may be bonded, e.g. adhered or welded to the catheter.

The catheter may be a urinary catheter. The catheter may be a male urinary catheter (i.e. a catheter for catheterisation of men). The catheter may be a female urinary catheter (i.e. a catheter for catheterisation of women). The catheter may be an intermittent catheter. The catheter may comprise a proximal end for insertion into the body and a distal end. In one embodiment, the catheter is an intermittent male urinary catheter. The features of the present invention allow intermittent urinary catheters to be used more easily and effectively.

The catheter may be formed of a material of the group comprising: polyvinyl chloride, polytetrafluoroethylene, polyolefins, latex, silicones, synthetic rubbers, polyurethanes, polyesters, polyacrylates, polyamides, thermoplastic elastomeric materials, styrene block copolymers, poly ether block amide, thermoplastic vulcanizates, thermoplastic copolyesters, thermoplastic polyamides, and water disintegrable or enzymatically hydrolysable material, or combinations, blends or copolymers of any of the above materials.

The water disintegrable or enzymatically hydrolysable material may comprise a material of the group comprising: polyvinyl alcohol, extrudable polyvinyl alcohol, polyacrylic acids, polylactic acid, polyesters, polyglycolide, polyglycolic acid, poly lactic-co-glycolic acid, polylactide, amines, polyacrylamides, poly(N-(2- Hydroxypropyl) methacrylamide), starch, modified starches or derivatives, amylopectin, pectin, xanthan, scleroglucan, dextrin, chitosans, chitins, agar, alginate, carrageenans, laminarin, saccharides, polysaccharides, sucrose, polyethylene oxide, polypropylene oxide, acrylics, polyacrylic acid blends, poly(methacrylic acid), polystyrene sulfonate, polyethylene sulfonate, lignin sulfonate, polymethacrylamides, copolymers of aminoalkyl-acrylamides and methacrylamides, melamine-formaldehyde copolymers, vinyl alcohol copolymers, cellulose ethers, poly-ethers, polyethylene oxide, blends of polyethylene- polypropylene glycol, carboxymethyl cellulose, guar gum, locust bean gum, hydroxypropyl cellulose, vinylpyrrolidone polymers and copolymers, polyvinyl pyrrolidone-ethylene-vinyl acetate, polyvinyl pyrrolidone- carboxymethyl cellulose, carboxymethyl cellulose shellac, copolymers of vinylpyrrolidone with vinyl acetate, hydroxyethyl cellulose, gelatin, poly-caprolactone, poly(p-dioxanone), or combinations, blends or co-polymers of any of the above materials.

Preferably, the intermittent catheter is formed of a polyolefin material, in particular polyethylene and/or polypropylene.

Preferably, the intermittent catheter is formed of a thermoplastic elastomeric material.

The catheter may comprise a proximal end for insertion into the body and a distal end. The distal end of the catheter may comprise a funnel. The funnel may be formed of a relatively rigid material compared to the rest of the catheter and/or fluid collection bag, for example high density poly-ethylene (HDPE). The funnel may have a truncated conical shape. The funnel may be joined to the distal end of the catheter at the narrow end of the funnel.

One or more, or each baffle may be provided by a join joining the front panel of the fluid collection bag to the rear panel of the fluid collection bag. Each join may comprise any one or more of: a weld; mechanical seal; heat seal; pressure seal; adhesive; solvent bond; ultraviolet bond; ultrasonic weld; laser weld; impulse weld; or friction weld. In a preferred embodiment, the join is a weld. Advantageously, the baffle can be easily formed and added to the fluid collection bag construction as part of conventional techniques for the manufacture of fluid collection bags. Alternatively, one or more, or each baffle may comprise a further panel, joined between the front panel and the rear panel. The joins joining the further panel may be any of the joins outlined above, i.e. any one or more of: a weld; mechanical seal; heat seal; pressure seal; adhesive; solvent bond; ultraviolet bond; ultrasonic weld; laser weld; impulse weld; or friction weld

Each baffle may create a fluid tight seal between the front panel and the rear panel. The internal cavity may be provided with at least 2 baffles, at least 3 baffles, at least 4 baffles, at least 5 baffles, at least 6 baffles, at least 7 baffles, at least 8 baffles, at least 9 baffles, or at least 10 baffles.

The internal cavity may be provided with no more than 2 baffles, no more than

3 baffles, no more than 4 baffles, no more than 5 baffles, no more than 6 baffles, no more than 7 baffles, no more than 8 baffles, no more than 9 baffles, or no more than 10 baffles.

The internal cavity may be provided with 2, 3, 4, 5, 6, 7, 8, 9 or 10 baffles. For example, the internal cavity may be provided with between 3 and 5 baffles, such as 4 baffles.

One or more, or each baffle may have a length equal to between about 5 % and about 80 %, between about 10 % and about 75 %, between about 15 % and about 70 %, between about 20 % and about 65 %, between about 25 % and about 60 %, between about 27.5 % and about 55 %, between about 30 % and about 50 %, between about 32.5 % and about 47.5 %, between about 35 % and about 45 %, between about 37.5 % and about 42.5 %, or equal to about 40 %, of the width of the fluid collection bag.

One or more, or each baffle may have a length equal to, or greater than, about 5% of the width of the fluid collection bag. Each baffle may have a length equal to, or greater than, about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 60%, about 65%, about 70%, about 75%, or equal to, or greater than, about 80%, of the width of the fluid collection bag.

One or more, or each baffle may have a length equal to no more than about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 60%, about 65%, about 70%, about 75%, or no more than about 80%, of the width of the fluid collection bag.

One or more, or each baffle may have a length of between about 1 and about 15 cm, between about 2 and about 13 cm, between about 3 and about 11 cm, between about

4 and about 10 cm, between about 4.5 and about 9 cm, between about 5 and about 8 cm, between about 5.5 and about 7 cm, or about 6 cm. One or more, or each baffle may have a length of at least about 1 cm, about 1.5 cm, about 2 cm, about 2.5 cm, about 3 cm, about 3.5 cm, about 4 cm, about 4.5 cm, about 5 cm, about 5.5 cm, about 6 cm, about 6.5 cm, or at least about 7 cm.

One or more, or each baffle may have a length of no more than about 1 cm, about 1.5 cm, about 2 cm, about 2.5 cm, about 3 cm, about 3.5 cm, about 4 cm, about 4.5 cm, about 5 cm, about 5.5 cm, about 6 cm, about 6.5 cm, or no more than about 7 cm.

The internal cavity may comprise a plurality of baffles each having a different length. Alternatively, the internal cavity may comprise a plurality of baffles each having the same length.

At least two of the plurality of internal baffles may be arranged as a diametrically opposed pair of baffles; a plurality of pairs of baffles may be arranged as diametrically opposed pairs of baffles. Each baffle may be arranged in a diametrically opposed pair of baffles. Each baffle of the diametrically opposed pairs of baffles may extend inwardly toward the opposing baffle in the pair to form a channel therebetween. Advantageously, the channel directs the flow of liquid entering the fluid collection bag at a flow rate in line with draining of a bladder, therefore, providing an improved flow of liquid through the internal cavity, thus facilitating filling of the bag through controlled liquid flow. On the other hand, the channel provided by the baffles restricts fast flow of the larger quantities of liquid that are provided in a partially filled fluid collection bag, preventing “sloshing” of the liquid within.

At the or each channel, the front panel is not joined to the rear panel, therefore, liquid is able to pass through the channel.

The diametrically opposed pairs of baffles may be arranged such that each pair is separated from an adjacent pair by a distance of between about 1 and about 20 cm, between about 2 and about 18 cm, between about 3 and about 16 cm, between about 4 and about 14 cm, between about 5 and about 12 cm, between about 6 and about 11 cm, between about 7 and about 10 cm, between about 7 and about 9 cm, or about 8 cm. Advantageously, the spacing between adjacent pairs of diametrically opposed baffles provides for an arrangement which does not unduly restrict the volume of the internal cavity of the bag whilst providing an improved flow of liquid into the internal cavity, therefore, reducing the risk of the bag overflowing with liquid during use.

The diametrically opposed pairs of baffles may be arranged such that each pair is separated from an adjacent pair by a distance of at least about 1 cm, about 2 cm, about 3 cm, about 4 cm, about 5 cm, about 6 cm, about 7 cm, about 8 cm, about 9 cm, or at least about 10 cm.

The diametrically opposed pairs of baffles may be arranged such that each pair is separated from an adjacent pair by a distance of no more than about 1 cm, about 2 cm, about 3 cm, about 4 cm, about 5 cm, about 6 cm, about 7 cm, about 8 cm, about 9 cm, or no more than about 10 cm.

The internal cavity may be provided with 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 diametrically opposed pairs of baffles.

The internal cavity may be provided with at least 1, 2, 3, 4, 5, 6, 7, 8, 9 or at least 10 diametrically opposed pairs of baffles.

The internal cavity may be provided with no more than 1, 2, 3, 4, 5, 6, 7, 8, 9 or no more than 10 diametrically opposed pairs of baffles.

The diameter of one or more or the or each channel (which where the channel is formed by a pair of opposing baffles may be defined as the shortest distance between the tips of the opposing baffles) may be equal to between about 5 % and about 80 %, between about 5 % and about 75 %, between about 5 % and about 70 %, between about 5 % and about 65 %, between about 5 % and about 60 %, between about 5 % and about 55 %, between about 5 % and about 50 %, between about 5 % and about 45 %, between about 5 % and about 40 %, between about 10 % and about 40 %, between about 10 % and about 35 %, between about 10 % and about 30 %, between about 10 % and about 25 %, between about 12.5 % and about 25 %, between about 15 % and about 25 %, between about 17.5% and about 25 %, between about 17.5 % and about 22.5 %, or equal to about 20%, of the width of the fluid collection bag. Advantageously, where the diameter of the channel is selected appropriately, the flow of liquid into the bag is improved by the liquid being directed to the bottom of the bag, and sloshing is impeded. The diameter of one or more or the or each channel may be equal to no more than about 5 %, about 7.5 %, about 10 %, about 12.5 %, about 15 %, about 17.5 %, about 20 %, about 22.5 %, about 25 %, about 27.5 %, about 30 %, about 35 %, about 40 %, about 45 %, about 50 %, about 55 %, about 60 %, about 65 %, about 70 %, about 75 %, about 80 %, about 85 %, or no more than about 90 % of the width of the fluid collection bag.

The diameter of one or more or the or each channel may be equal to at least about 5 %, about 7.5 %, about 10 %, about 12.5 %, about 15 %, about 17.5 %, about 20 %, about 22.5 %, about 25 %, about 27.5 %, about 30 %, about 35 %, about 40 %, about 45 %, about 50 %, about 55 %, about 60 %, about 65 %, about 70 %, about 75 %, about 80 %, about 85 %, or at least about 90 % of the width of the fluid collection bag.

The diameter of one or more or the or each channel may be between about 0.5 and about 5 cm, between about 0.75 and about 4.5 cm, between about 1 and about 4 cm, between about 1.25 and about 3.5 cm, between about 1.5 and about 3 cm, between about 1.5 and about 2.5 cm, between about 1.75 and about 2.25 cm, or about 2 cm.

The diameter of one or more or the or each channel may be at least about 0.25 cm, about 0.5 cm, about 0.75 cm, about 1 cm, about 1.25 cm, about 1.5 cm, about 1.75 cm, about 2 cm, about 2.25 cm, about 2.5 cm, about 2.75 cm, about 3 cm, about 3.25 cm, about 3.5 cm, about 3.75 cm, about 4 cm, about 4.25 cm, about 4.5 cm, about 4.75 cm, or at least about 5 cm.

The diameter of one or more or the or each channel may be no more than about 0.25 cm, about 0.5 cm, about 0.75 cm, about 1 cm, about 1.25 cm, about 1.5 cm, about

1.75 cm, about 2 cm, about 2.25 cm, about 2.5 cm, about 2.75 cm, about 3 cm, about 3.25 cm, about 3.5 cm, about 3.75 cm, about 4 cm, about 4.25 cm, about 4.5 cm, about

4.75 cm, or no more than about 5 cm.

Each baffle of a diametrically opposed pair of baffles may be the same length. Alternatively, each baffle of a diametrically opposed pair of baffles may be a different length. Each diametrically opposed pair of baffles may comprise baffles the same length. Alternatively the baffles in one diametrically opposed pair of baffles may be a different length to that of another diametrically opposed pair of baffles.

In one embodiment, the plurality of baffles are arranged as two pairs of diametrically opposed pairs of baffles, wherein each baffle extends inwardly toward the corresponding baffle in its pair to form a channel therebetween. In this example, the diameter of the channel is equal to about 20% of the width of the fluid collection bag, and each baffle of each diametrically opposed pair of baffles has a length equal to about 40 % of the width of the fluid collection bag.

The bond may be a peripheral bond. The peripheral bond may define a base, two lateral edges and an upper edge of the fluid collection bag. The two lateral edges may comprise a right lateral edge and a left lateral edge. The right lateral edge and left lateral edge may be defined as the right and left sides of the bag when viewing the bag with the rear panel behind the front panel, the base at the bottom of the bag and the upper edge at the top of the bag. The bag may have a width between the left lateral edge and right lateral edge of at least 10, 12, 15 or 20 cm. The bag may have a width no more than 25, 20, or 15 cm. Preferably, the width is between 10 and 20 cm, more preferably between 15 and 18 cm, and most preferably about 17 cm. The base may define a bottom of the bag. The upper edge may define a top of the bag. The height of the bag from the base to the upper edge may be at least 25, 30, 35 or 40 cm. The height of the bag may be no more than 45, 40, 35 or 30 cm. The height may be between 25 and 40 cm, 32 and 38 cm, or most preferably 34 and 37 cm. The bag may be configured to hold at least 500, 700, or 1000 ml of fluid, and may hold no more than 1000 ml, for example, it may hold at least 700 ml of fluid.

In an example embodiment, the fluid collection bag may comprise a number of baffles extending from the left lateral edge and a number of baffles extending from the right lateral edge. The example embodiment is particularly advantageous where the fluid collection bag comprises an inlet configured to receive fluid from the catheter arranged at an upper edge of the fluid collection bag. For example, the bag may comprise two baffles extending from the left lateral edge and two baffles extending from the right lateral edge. The four baffles may be arranged as diametrically opposed pairs of baffles, such that a first baffle extending from the left lateral edge and a first baffle extending from the right lateral edge are a first diametrically opposed pair, and a second baffle extending from the left lateral edge and a second baffle extending from the right lateral edge are a second diametrically opposed pair. The first diametrically opposed pair of baffles may form a channel therebetween, and the second diametrically opposed pair of baffles may form a channel therebetween.

The internal cavity may comprise at least one baffle arranged to form a channel between one end, or both ends, of the baffle and the bond. For example, the internal cavity may comprise at least one baffle having an end arranged proximal to the upper edge, left lateral edge, base or right lateral edge of the peripheral bond and forming a channel between the end of the baffle and an aforementioned part of the bond. This channel may comprise any of the dimensions described above.

The fluid collection bag may be provided in a stowed configuration. In the stowed configuration, the fluid collection bag may be folded or rolled to reduce its size in any one dimension. The stowed configuration may be a folded or rolled configuration. Thus, the size of the fluid collection bag is minimised inside the pouch and this assists the user in removing the bag and other elements of the packaged catheter assembly from the pouch. The stowed configuration of the fluid collection bag inhibits fluid flow onto the exterior surface of the fluid collection bag as it must penetrate between folds.

The bond may comprise any one or more of: a weld; mechanical seal; heat seal; pressure seal; adhesive; solvent bond; ultraviolet bond; ultrasonic weld; laser weld; impulse weld; or friction weld.

The fluid collection bag may comprise a flexible plastics material. For example, polypropylene (PP), polyethylene terephthalate (PET), low density polyethylene (LDPE), metalized polyester (MET PET) orientated polypropylene (OPP), or polyvinyl chloride (PVC). At least part of the fluid collection bag may be transparent or translucent. The front panel of the fluid collection bag may be transparent or translucent. Thus, the fluid collection bag can conform to the shape of the catheter assembly, is convenient to carry and also provides a visual reference to the contents of the bag before, during and after use which makes it easier to use. At least one, preferably each, of the baffles may extend inwardly from the bond, i.e. at least one baffle originates at the bond and extends inwardly therefrom.

Each baffle may extend inwardly from any part of the bond. Preferably, each of the baffles extend inwardly from the left lateral edge or the right lateral edge.

At least one of the baffles may extend inwardly from the left lateral edge or right lateral edge at a distance equal to about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90% or about 95% of the distance from the base to the upper edge.

At least one of the baffles may extend inwardly from the left lateral edge or right lateral edge at a distance equal to at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90% or at least about 95% of the distance from the base to the upper edge.

At least one of the baffles may extend inwardly from the left lateral edge or right lateral edge at a distance equal to no more than about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90% or no more than about 95% of the distance from the base to the upper edge.

At least one of the baffles may extend inwardly from the base or upper edge at a distance equal to about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90% or about 95% of the distance from the left lateral edge to the right lateral edge.

At least one of the baffles may extend inwardly from the base or upper edge at a distance equal to at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90% or at least about 95% of the distance from the left lateral edge to the right lateral edge. At least one of the baffles may extend inwardly from the base or upper edge at a distance equal to no more than about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90% or no more than about 95% of the distance from the left lateral edge to the right lateral edge.

At least one of the baffles may extend inwardly from the left lateral edge a distance equal to about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90% or about 95% of the distance between the left lateral edge and the right lateral edge.

At least one of the baffles may extend inwardly from the right lateral edge a distance equal to about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90% or about 95% of the distance between the right lateral edge and the left lateral edge.

At least one of the baffles may extend inwardly from the left lateral edge a distance equal to at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90% or at least about 95% of the distance between the left lateral edge and the right lateral edge.

At least one of the baffles may extend inwardly from the right lateral edge a distance equal to at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90% or at least about 95% of the distance between the right lateral edge and the left lateral edge.

At least one of the baffles may extend inwardly from the left lateral edge a distance equal to no more than about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90% or no more than about 95% of the distance between the left lateral edge and the right lateral edge. At least one of the baffles may extend inwardly from the right lateral edge a distance equal to no more than about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90% or no more than about 95% of the distance between the right lateral edge and the left lateral edge.

At least one of the baffles may extend inwardly from the base a distance equal to about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90% or about 95% of the distance between the base and the upper edge.

At least one of the baffles may extend inwardly from the upper edge a distance equal to about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90% or about 95% of the distance between the upper edge and the base.

At least one of the baffles may extend inwardly from the base a distance equal to at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90% or at least about 95% of the distance between the base and the upper edge.

At least one of the baffles may extend inwardly from the upper edge a distance equal to at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90% or at least about 95% of the distance between the upper edge and the base.

At least one of the baffles may extend inwardly from the base a distance equal to no more than about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90% or no more than about 95% of the distance between the base and the upper edge. At least one of the baffles may extend inwardly from the upper edge a distance equal to no more than about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90% or no more than about 95% of the distance between the upper edge and the base.

At least one, preferably each, baffle may extend inwardly from the bond at an angle perpendicular, i.e., substantially perpendicular, at about 90° to the bond. Advantageously, this arrangement provides an improved flow of liquid through the internal cavity, thus facilitating filling of the bag.

At least one, preferably each, baffle may extend inwardly from the bond at an angle of between about 5° and about 175°, between about 10° and about 170°, between about 15° and about 165°, between about 20° and about 160°, between about 25° and about 155°, between about 30° and about 150°, between about 35° and about 145°, between about 40° and about 140°, between about 45° and about 135°, between about 50° and about 130°, between about 55° and about 125°, between about 60° and about 120°, between about 65° and about 115°, between about 70° and about 110°, between about 75° and about 105°, between about 80° and about 100°, between about 85° and about 95°, or about 90°, relative to the bond.

At least one, preferably each, baffle may extend inwardly from the bond at an angle of at least about 5°, about 10°, about 15°, about 20°, about 25°, about 30°, about 35°, about 40°, about 45°, about 50°, about 60°, about 65°, about 70°, about 75°, about 80°, about 85°, or at least about 90°, relative to the bond.

At least one, preferably each baffle may extend inwardly from the bond at an angle of no more than about 5°, about 10°, about 15°, about 20°, about 25°, about 30°, about 35°, about 40°, about 45°, about 50°, about 60°, about 65°, about 70°, about 75°, about 80°, about 85°, or no more than about 90°, relative to the bond.

The plurality of baffles may be arranged in a regular arrangement. For example, each baffle in a plurality of pairs of baffles may extend by the same distance from the peripheral bond so as to define a plurality of channels each in alignment along the centreline of the fluid collection bag. Alternatively, the plurality of internal baffles may be arranged in a random, or scattered arrangement. By this, we mean that the internal cavity does not comprise an identifiable channel formed between adjacent baffles. Such an arrangement provides for separation of the panels of the fluid collection bag, therefore, facilitating the infill of liquid.

The fluid collection bag may be any suitable shape or size, for example rectangular, circular, elliptical, cuboid, spherical, etc, preferably rectangular.

The fluid collection bag may comprise an interaction region as described below in relation to the second aspect of the invention. The interaction region of the fluid collection bag may be used to facilitate pouring away or discarding of the contents of the bag, or for allowing access to the contents of the bag.

The fluid collection bag may comprise an inlet to allow fluid to enter the bag from the distal end of the catheter. The inlet may comprise a one-way valve which prevents fluid flow through the inlet from the fluid collection bag to the catheter. Thus, the inlet allows liquid to pass into the fluid collection bag but prevents fluid flow out of the bag and into the catheter. This can reduce the likelihood of leaking. Preferably, the inlet is located at an upper edge of the fluid collection bag (the upper edge of the fluid collection bag may be defined as the end where the inlet is located). The inlet may be located at the end of a spout. The spout may extend from the upper edge, left lateral edge, base or right lateral edge of the bag, but preferably from the upper edge. The spout may taper inwardly as it extends away from the fluid collection bag. The spout may comprise an end, distal to the fluid collection bag, which comprises the inlet. The spout may have a length, i.e., the distance from where the spout joins an edge of the fluid collection bag to the inlet, of between 2 and 14 cm, between 4 and 12 cm, between 6 and 10 cm, between 7 and 9 cm, or about 8 cm.

Advantageously, the spout makes it easier for the user to locate the inlet and provides a more secure connection between the catheter and the fluid collection bag. The spout may also facilitate draining of the contents of the fluid collection bag after use.

The pouch may be divided into first and second compartments. The fluid reservoir and at least a portion of the catheter may be arranged in the first compartment. The fluid collection bag may be connected to the catheter and arranged in the second compartment. The fluid reservoir may be configured to release the wetting fluid into the first compartment to wet the catheter. The pouch may comprise an interaction region operable by a user to form an opening in the pouch allowing access to at least the second compartment

According to a second aspect of the invention, there is provided a packaged catheter assembly comprising a catheter, a fluid reservoir comprising wetting fluid, and a pouch, wherein: the pouch is divided into first and second compartments; the fluid reservoir and at least a portion of the catheter are arranged in the first compartment; and a fluid collection bag is connected to the catheter and is arranged in the second compartment; and the fluid reservoir is configured to release the wetting fluid into the first compartment to wet the catheter.

With this arrangement, a substantial amount, if not all, of the wetting fluid remains in the first compartment upon release of the wetting fluid from the fluid reservoir. Advantageously, this means that the fluid collection bag remains dry and free from wetting fluid prior to use. Beneficially, for the user, in particular for users with limited dexterity, this means handling and re-packaging of the bag during and after use is considerably easier than if the bag is wetted with wetting fluid.

Further advantageously, the wetting fluid is retained in the first compartment comprising at least a portion of the catheter and is not distributed amongst the components in the second compartment of the pouch. This may be the case even where the pouch is vigorously shaken to distribute the wetting fluid within it. This means that all of the wetting fluid, or at least a substantial amount of the wetting fluid, is available to wet the catheter prior to use, as is intended. Beneficially, this arrangement ensures that there is sufficient wetting fluid to activate the whole catheter surface, therefore, preventing discomfort and injury during use.

The pouch may comprise an interaction region operable by a user to form an opening in the pouch allowing access to at least the second compartment.

Accordingly in one embodiment, there is provided a packaged catheter assembly comprising a catheter, a fluid reservoir comprising wetting fluid, and a pouch, wherein: the pouch is divided into first and second compartments; the fluid reservoir and at least a portion of the catheter are arranged in the first compartment; and a fluid collection bag is connected to the catheter and is arranged in the second compartment; and the fluid reservoir is configured to release the wetting fluid into the first compartment to wet the catheter; and the pouch comprises an interaction region operable by a user to form an opening in the pouch allowing access to at least the second compartment

The opening may allow access to the first compartment. Access to the first compartment may be via the second compartment. Beneficially, this means that the fluid collection bag is withdrawn from the pouch through the opening before the catheter. Thus, the user does not need to touch the wetted catheter before touching the fluid collection bag, therefore, preventing accidental wetting of the fluid collection bag during withdrawal of the components from the pouch.

The pouch may comprise two walls (a front wall and a rear wall). The pouch may comprise a peripheral seal between the two walls. The pouch may comprise a front wall and a rear wall, a peripheral seal between the two walls, and an internal join, joining the walls to divide the pouch into the first and second compartments. Advantageously, this arrangement requires only minor modifications to existing packaged catheter assembly manufacturing techniques as the internal join can be formed simultaneously with the peripheral seal. Further, the first and second compartments are formed without the need for additional components to be contained within the pouch, which otherwise may act to obstruct withdrawal of the fluid collection bag and catheter from the pouch, and may inhibit wetting of the catheter.

The peripheral seal may provide a sterile seal. Thus, the pouch may maintain the sterility of its contents.

The peripheral seal may form one or more edges of the pouch. The peripheral seal may comprise a left lateral edge, right lateral edge, an upper edge and a base of the pouch. The left and right lateral edges may be defined as the left and right edges when viewing the pouch with the front wall in front of the rear wall, the base at the bottom and the upper edge at the top. The pouch may be any suitable shape such as circular, elliptical, triangular, tubular, prismatic or polygon, preferably the pouch is rectangular. The pouch may have a width defined as the distance between the left lateral edge and right lateral edge of the pouch of at least 60, 70, 80, 90, 100, 110, 120, 130, 140, 150, 160, 170 or 180 mm. The pouch may have a width of no more than 200, 190, 180, 170, 160, 150, 140, 130, 120, 110, 100, 90, 80, or 70 mm. Preferably, the width is between 120 and 170 mm, and most preferably about 130-150 mm, for example 136 mm. The pouch may have a height defined as the distance between the upper edge and base of at least 60, 70, 80, 90, 100, 125, 150, 175, 200 or 225 mm. The pouch may have a height of no more than 250, 225, 200, 175, 150, 125, 110, 100, 90, 80, or 70 mm. Preferably, the height is between 80 and 200 mm, and most preferably it is about 90-180 mm, for example 174 mm or 90 mm. The peripheral seal may comprise any one or more of: a weld; mechanical seal; heat seal; pressure seal; adhesive; solvent bond; ultraviolet bond; ultrasonic weld; laser weld; impulse weld; or friction weld. The peripheral seal may be re- sealable, for example through a resealable adhesive, an additional adhesive that is activated prior or during resealing, or a hook and loop/hook and hook fastener. Thus, the peripheral seal can be easily constructed to suit the specific needs of the pouch.

The internal join may comprise any one or more of: a weld; mechanical seal; heat seal; pressure seal; adhesive; solvent bond; ultraviolet bond; ultrasonic weld; laser weld; impulse weld; or friction weld. Preferably, the internal join comprises a weld. Thus, advantageously, existing manufacturing techniques may be adapted to form the internal join.

The peripheral seal may provide a water-tight seal.

The internal join may provide a water-resistant or water tight seal. Advantageously, a water resistant seal inhibits the passage of wetting fluid from the first compartment through the internal join to the second compartment, whilst a watertight seal prevents the passage of wetting fluid from the first compartment, through the internal join, into the second compartment. Thus, the fluid collection bag which is arranged in the second compartment remains dry.

The internal join may be arranged to inhibit wetting fluid from the fluid reservoir wetting the second compartment and the fluid collection bag arranged therein. Advantageously, this means that the fluid collection bag remains dry prior to use. Beneficially, for the user, in particular for users with limited dexterity, this means handling and re-packaging of the bag during and after use is considerably easier than if the bag is wetted with wetting fluid.

Moreover, this arrangement allows a user to vigorously shake the pouch after wetting fluid is released from the fluid reservoir, therefore, ensuring distribution of wetting fluid to the catheter without the risk of wetting the fluid collection bag. Beneficially, this ensures that there is sufficient wetting fluid to activate the whole catheter surface, therefore, preventing, or at least significantly reducing, discomfort and injury during use.

A catheter assembly may comprise a catheter tube and a fluid collection bag. The internal join may define a channel having a diameter which is substantially equal to, or greater than, the diameter of the catheter at the channel. The catheter may be arranged such that before withdrawal of the catheter from the pouch, a portion of the catheter is positioned within the channel. Preferably, the internal join may define a channel having a diameter which is substantially equal to, or greater than, the diameter of the catheter tube, and that before withdrawal of the catheter from the pouch, the catheter tube is positioned within the channel. Preferably, a portion of the distal end of the catheter tube is positioned within the channel. Alternatively, the catheter assembly may comprise a connector arranged to connect the distal end of the catheter to the fluid collection bag. In this case, if the connector is arranged in the channel then the diameter of the channel may be substantially equal to, or greater than, the diameter of the connector or gripping element.

Advantageously, this arrangement provides for a connection between the fluid collection bag and the catheter which does not impact the ability of the pouch to retain the wetting fluid in the first compartment. Thus, the fluid collection bag remains dry prior to use. Moreover, typically, a catheter is of sufficient length such that the distal end of the catheter is not required to be inserted into the body during use. Thus, in embodiments where a portion of the distal end of the catheter tube is positioned in the channel, it is not essential for this portion of the catheter to be wetted by the wetting fluid. As such, the catheter tube can be positioned within the channel without having a detrimental effect on the use of the catheter. The interaction region may define a first point of contact for a user of the packaged catheter assembly. The interaction region may facilitate user access to the contents of the pouch. The opening may be in or near an upper edge of a peripheral seal of the pouch. The opening may allow access to the second compartment. The opening may allow access to the first compartment via the second compartment. The catheter may be withdrawn through the opening, for example via the second compartment. Thus, access to the pouch may be provided adjacent to the second compartment and as such, the wetting fluid in the first compartment is retained in the pouch while the catheter is withdrawn via the second compartment, therefore reducing the risk of spilling wetting fluid outside the pouch or contacting the fluid collection bag with wetting fluid.

The interaction region may comprise a breakable region of a peripheral seal of the pouch. The method may comprise forming a breakable region in the peripheral seal. The breakable region may comprise a tear-away region which may comprise a tear line defining a line along which the pouch may be tom to at least partially separate the tearaway region from the remainder of the pouch, thereby creating the opening in the peripheral seal. The tear-away region may comprise a tear start. The tear start may be provided at a first end of the tear-away region. The tear start may comprise a notch, or area of weakness, in one or both of the walls of the pouch. The tear start may define the first part of the pouch to be tom. The tear-away region may comprise a tear stop. The tear stop may be provided at a second end of the tear-away region. The tear stop may act to prevent or reduce the likelihood of the tear-away region being completely separated from the remainder of the packaging. A tear line may be defined between the tear start and the tear stop. The tear line may be configured to preferentially tear. The tear line may comprise a weakened region of the pouch. The tear line may be formed by any suitable means, such as laser scoring. Thus the breakable region provides a convenient and easy means to open the pouch with minimal effort and no additional equipment/tools.

The interaction region may comprise an aperture or pull tab. The aperture may be sized to allow a finger to pass through and grip the interaction region. The pull tab may be sized to allow a user to grip it between their thumb and index finger. Preferably, the aperture or pull tab is located in the tear-away region. The aperture or pull tab may be located on the same side of the pouch as the tear start. The aperture or pull tab may be located adjacent to the tear start. The aperture may be any suitable shape, for example, circular, elliptical, square or irregularly shaped. Preferably, the aperture is circular. Thus, the user can more easily grasp the tear-away region and open the pouch.

The interaction region may be arranged at one edge of the pouch.

The channel may be arranged adjacent to the interaction region. Advantageously, where the catheter is positioned within the channel, this means that it is easier for a user to withdraw the catheter from the pouch as the catheter is adjacent to the interaction region which forms the opening in the pouch. In particular, this arrangement facilitates removal of the catheter by withdrawing the fluid collection bag, therefore, removing the need for the user to touch the catheter. This prevents the catheter becoming dirty and also means the healthcare professional or user avoids touching the wetting fluid on the catheter which could be transferred to the fluid collection bag, therefore, making handling of the fluid collection bag difficult.

The internal join may be linear. The internal join may be elongated. The internal join may comprise a first end and a second end. The internal join may be curved, for example an ‘S’-shape or a ‘U’-shape.

The internal join may extend from the peripheral seal to the channel. Preferably, the internal join extends from the peripheral seal to the channel on an edge other than that where the interaction region is provided and most preferably opposite the interaction region. This arrangement facilitates withdrawal of the catheter and fluid collection bag from the pouch.

The internal join may extend toward the interaction region from its first end at the peripheral seal, for example from the left lateral edge, upper edge, right lateral edge base, at a corner where the upper edge and the left lateral edge meet, at a comer where the left lateral edge and base meet, at a comer where the base and the right lateral edge meet, or at a comer where the right lateral edge and the upper edge meet. The internal join may terminate at its second end. The second end may be positioned anywhere within the pouch, for example joined to any part of the peripheral seal or proximal to the upper edge, left lateral edge, base or right lateral edge. Preferably, the second end of the internal join is positioned proximal to the interaction region. Preferably, the second end is positioned approximately mid-way between the base and upper edge of the peripheral seal proximal to the right lateral edge of the pouch.

When viewing the pouch with the front wall in front of the rear wall, the second compartment may be any shape, for example triangular, rectangular, square, trapezoidal or irregularly shaped. The second compartment may be bordered by any of the edges of the fluid collection bag and the internal join. The second compartment may be triangular and may be bordered by the, or a portion of the, upper edge, left lateral edge, base, right lateral edge or internal join. For example, the second compartment may be triangular and bordered by the upper edge, internal join and part of, e.g. approximately half of the length of a lateral edge, e.g. the right lateral edge. This is particularly preferred where the interaction region is arranged at the same lateral edge that forms the triangular compartment.

When viewing the pouch with the front wall in front of the rear wall, the first compartment may be any shape, for example triangular, rectangular, square, trapezoidal or irregularly shaped. The first compartment may be bordered by any of the edges of the fluid collection bag and the internal join. The first compartment may be bordered by the, or a portion of the, upper edge, left lateral edge, base, right lateral edge or internal join. For example, the first compartment may be bordered by the left lateral edge, base, internal join and approximately half of the length of the right lateral edge.

The internal join may have a length substantially equal to the width of the pouch and/or may span approximately the entire width of the pouch.

The internal join may have a length of between about 2 and about 28 cm, between about 4 and about 26 cm, between about 6 and about 24 cm, between about 8 and about 22 cm, between about 10 and about 20 cm, between about 11 and about 18 cm, between about 12 and about 16 cm, between about 13 and about 15 cm, or about 14 cm.

The internal join may have a length of at least about 1 cm, about 2 cm, about 3 cm, about 4 cm, about 5 cm, about 6 cm, about 7 cm, about 8 cm, about 9 cm, about 10 cm, about 11 cm, about 12 cm, about 13 cm, about 14 cm, about 15 cm, about 16 cm, about 17 cm, about 18 cm, about 19 cm, about 20 cm, about 21 cm, about 22 cm, about 23 cm, about 24 cm, about 25 cm, about 26 cm, about 27 cm, or at least about 28 cm.

The internal join may have a length of no more than about 1 cm, about 2 cm, about 3 cm, about 4 cm, about 5 cm, about 6 cm, about 7 cm, about 8 cm, about 9 cm, about 10 cm, about 11 cm, about 12 cm, about 13 cm, about 14 cm, about 15 cm, about 16 cm, about 17 cm, about 18 cm, about 19 cm, about 20 cm, about 21 cm, about 22 cm, about 23 cm, about 24 cm, about 25 cm, about 26 cm, about 27 cm, or no more than about 28 cm.

The internal join may have a width of between about 0.2 and about 2 cm, between about 0.3 and about 1.8 cm, between about 0.4 and about 1.6 cm, between about 0.5 and about 1.4 cm, between about 0.6 and about 1.2 cm, between about 0.7 and about 1.0 cm, between about 0.75 and about 0.95 cm, between about 0.75 and about 0.90 cm, between about 0.75 and about 0.85 cm, or about 0.80 cm.

The internal join may have a width of at least about 0.10 cm, about 0.15 cm, about 0.20 cm, about 0.25 cm, about 0.30 cm, about 0.35 cm, about 0.40 cm, about 0.45 cm, about 0.50 cm, about 0.55 cm, about 0.60 cm, about 0.65 cm, about 0.70 cm, about 0.75 cm, about 0.80 cm, about 0.85 cm, about 0.90 cm, about 0.95 cm, or at least about 1.00 cm.

The internal join may have a width of no more than about 0.10 cm, about 0.15 cm, about 0.20 cm, about 0.25 cm, about 0.30 cm, about 0.35 cm, about 0.40 cm, about 0.45 cm, about 0.50 cm, about 0.55 cm, about 0.60 cm, about 0.65 cm, about 0.70 cm, about 0.75 cm, about 0.80 cm, about 0.85 cm, about 0.90 cm, about 0.95 cm, or no more than about 1.00 cm.

The channel may have a diameter defined by the distance between the second end of the internal join and an inner perimeter of the peripheral seal adjacent to the second end. Preferably, the channel has a diameter defined by the distance between the second end of the internal join and the inner perimeter of the right lateral edge.

The catheter may have a diameter of between CH8 and CH 18, for example CH14 as defined by the French Scale system. The channel may have a diameter of between about 0.1 and about 1 cm, between about 0.2 and about 0.9 cm, between about 0.25 and about 0.8 cm, between about 0.3 and about 0.75 cm, between about 0.35 and about 0.7 cm, between about 0.4 and about 0.65 cm, between about 0.42 and about 0.6 cm, between about 0.44 and about 0.55 cm, between about 0.46 and about 0.52, between about 0.48 and about 0.51 cm, or about 0.5 cm.

The channel may have a diameter of at least about 0.10 cm, about 0.15 cm, about 0.20 cm, about 0.25 cm, about 0.30 cm, about 0.35 cm, about 0.40 cm, about 0.45 cm, about 0.50 cm, about 0.55 cm, about 0.60 cm, about 0.65 cm, about 0.70 cm, about 0.75 cm, about 0.80 cm, about 0.85 cm, about 0.90 cm, about 0.95 cm, or at least about 1.00 cm.

The channel may have a diameter of no more than about 0.10 cm, about 0.15 cm, about 0.20 cm, about 0.25 cm, about 0.30 cm, about 0.35 cm, about 0.40 cm, about 0.45 cm, about 0.50 cm, about 0.55 cm, about 0.60 cm, about 0.65 cm, about 0.70 cm, about 0.75 cm, about 0.80 cm, about 0.85 cm, about 0.90 cm, about 0.95 cm, or no more than about 1.00 cm.

Because of the dimensions of the internal join and channel, in embodiments where the catheter is positioned within the channel, the catheter may be held within the channel on one side by the internal join and on the other side by the peripheral seal. Advantageously, this means that ingress of wetting fluid through the channel into the second compartment is significantly inhibited as the channel is obstructed by the catheter. Thus, the fluid collection bag remains dry prior to use.

The channel may be tapered. The channel may extend upwards more on one side than the other. The channel may extend upwards more on the side corresponding to the terminus of the internal join. The channel may extend upwards no more than 200%, 100%, 75%, or 50% more on one side than the other. The channel may extend upwards at least 25%, 50%, 75%, 100%, or 150% more on one side than the other.

The pouch may be divided into more than two compartments, for example three compartments, four compartments, or more compartments, and each compartment may be separated from its adjacent compartment(s) by an internal join. Each compartment may comprise a different component of the catheter assembly.

The pouch may be configured such that after release of the wetting fluid into the first compartment, the wetting fluid is retained in the first compartment and the second compartment remains free, or at least substantially free, from wetting fluid.

‘Substantially free’ may be defined as having less than 5% of the wetting fluid reaching the second compartment after rupturing the fluid reservoir and vigorously shaking the pouch for five seconds.

Advantageously, this means that the fluid collection bag remains dry prior to use. Beneficially, for the user, in particular for users with limited dexterity, this means handling and re-packaging of the bag during and after use is considerably easier than if the bag is wetted with wetting fluid.

Moreover, this arrangement allows a user to vigorously shake the pouch after wetting fluid is released from the fluid reservoir, therefore, ensuring distribution of wetting fluid to the catheter without the risk of wetting the fluid collection bag. Beneficially, this ensures that there is sufficient wetting fluid to activate the whole catheter surface, therefore, preventing discomfort and injury during use.

The interaction region may be configured such that before withdrawal of the catheter from the pouch, the opening comprises a sterile seal. Beneficially, this ensures that the catheter is maintained within a sterile environment prior to use.

The sterile seal may be broken by tearing off a removable tear strip. Advantageously, this provides an easy way of opening the pouch and provides no obstacle or restriction to opening the pouch to a user with limited dexterity.

Actuation of the interaction region may create an opening in the pouch. The interaction region may be a break-away region such as a peel-away or tear-away region configured to be at least partially separated from the pouch. The catheter may be withdrawn through the opening. Before withdrawal of the catheter from the pouch, the opening may comprise a sterile seal. The sterile seal may be broken by actuation of the interaction region, for example by peeling a peel-away region from the pouch. The break-away region may form a part of the walls of the pouch, for example, the break-away region may form a part of the front wall. Preferably, the break-away region forms a majority of the front wall. The break-away region may be any suitable shape or size, for example, rectangular, circular, ellipsoidal or irregularly shaped. Preferably, the break-away region is the same shape as the pouch, for example rectangular. The break-away region may comprise a base, left lateral edge, right lateral edge and upper edge that form the edges of the interaction region. The edges of the interaction region may correspond to the respective edges of the pouch. The breakaway region may comprise a width between its left lateral edge and right lateral edge. The width of the break-away region may be at least 50%, 60%, 70%, 80% or 90% of the width of the pouch, for example, between 50-100%, 70-90% or 80-90% of the width of the pouch, most preferably the break-away region has a width of 85% of the width of the pouch. The break-away region may comprise a height between its base and upper edge. The height of the break-away region may be at least 50%, 60%, 70%, 80% or 90% the height of the pouch, for example between 50-100%, 60-90% or 70-80% of the height of the pouch, most preferably 75% of the height of the pouch. The break-away region may be positioned centrally with respect to the width and/or height of the pouch. Alternatively, the break-away region may have a different shape to the pouch and may not be positioned centrally with respect to the width and/or height of the pouch. Thus, the break-away region can be configured in many different ways to provide easy access to the contents of the pouch.

The break-away region may comprise rounded edges. Thus, the break-away region has a smoother and less jagged appearance.

The break-away region may formed of the same material as the walls of the pouch. This may ensure that the pouch has a consistent feel to the user and also that one area of the pouch is not weaker than the rest. Of course, in some embodiments, the break-away region may be formed of a different material to the rest of the pouch, for example where certain mechanical properties/tactile feel of the break-away region are desired.

The break-away region may be the same colour, a different shade of colour or a different colour to the rest of the pouch. Preferably, the break-away region is a different shade of colour, or different colour, to the rest of the pouch. This makes it more visually recognisable.

The pouch may comprise an access aperture. The access aperture may be positioned in one wall of the pouch, for example, the front wall. The break-away region may be configured to cover and/or seal the access aperture. The break-away region may be attached to the pouch by any suitable bonding/sealing method, for example chemical adhesives, chemical bonding, ultrasonic bonding, or mechanical bonding. This arrangement is preferred where the break-away region is a peel-away region, as the sealing/bonding method can be selected to allow the peel-away region to be peeled away. The break-away region may be formed from the same piece of material as a wall of the pouch. A line of weakness or tear-line in the pouch may define the break-away region. This arrangement is preferred where the break-away region is a tear-away region, as the tear-away region can be torn away along the line of weakness/tear line. Thus the user to form an opening in the pouch/reveal the access aperture by separating the break-away region from the pouch.

An edge of the break-away region may be both part of the break-away region and part of a wall (e.g. front wall) of the pouch. Thus, a fold-line may be defined at the edge of the break-away region. The break-away region may pivot to allow access to the pouch. The break-away region may be configured to remain connected to the pouch. This reduces the number of items that the user must worry about during use of the catheter assembly which makes it more convenient and easier to use.

The fold-line may correspond to the upper edge of the break-away region, thus the break-away region swings upwards away from the base of the pouch. The fold-line may correspond to the base of the break-away region, thus the break-away region swings down away from the upper edge of the pouch. In some embodiments, the foldline may correspond to a lateral edge of the break-away region allowing the break-away region to provide a door into the pouch. Thus, the break-away region can be flexibly configured to provide access to the pouch in many different ways.

The fluid collection bag may be attached to the break-away region, for example by the retaining element as described above. The break-away region may be configured to remove the fluid collection bag from the pouch during opening of the pouch. This makes it easier to access the fluid collection bag.

The pouch may comprise a tab. The tab may extend from an edge of the pouch/break-away region. The tab may be configured to create an opening in the peripheral seal of the pouch, for example through (partial) separation of the break-away region and pouch. Thus, the pouch can be more easily opened.

The tab may extend from one (i.e. the front or rear) wall of the pouch. The tab may be configured to fold down to overlie a (rear or preferably front) wall of the pouch. The tab may be configured to seal to a (rear or preferably front) wall of the pouch. Thus, the folded tab does not extend out and increase the bulk of the pouch.

The tab may span the majority of the width of the pouch, for example the entire width of the pouch. The tab may be triangular. A tip of the tab may extend down about half the height of the pouch. The tab may give the closed pouch the appearance of a closed envelope. Thus, the pouch has a familiar appearance that the user will recognise and be able to open easily.

Preferably, one wall comprises the break-away region. A tab may be provided on the break-away region. A tab may extend from an edge of the pouch. The tab may be configured to be separate from the pouch to create an opening in the peripheral seal of the pouch. Advantageously, the tab extends from the pouch and so is easy to grasp by the user. This makes opening the pouch easy even for users with reduced mobility.

The tab may comprise a front opening tab. The front opening tab may be attached to the break-away region. The front opening tab may overlie the pouch and preferably the front opening tab overlies an edge of the pouch. The front opening tab may be smaller an edge of the pouch. Thus, the tab can be easily identified and separated to open the pouch.

The tab may comprise an opening marker. The opening marker may be configured to provide a visual/tactile guide to the user to prompt them to open the pouch. The opening marker may comprise an arrow, or a pointed shape such as a triangle. The opening marker may prompt the user to pull or move the tab to open the pouch. The arrow may point in the direction the tab should be opened. Preferably, an opening marker is provided on the tab connected to the break-away region. Thus, the pouch is more user friendly.

The tab may extend from an edge of the pouch that corresponds to a frangible portion of the peripheral seal. Thus, the tab is suitably located to ensure the frangible portion breaks when the tab and pouch are separated.

The tab may be configured to provide a handling point for the pouch. Thus, the tab can be used to conveniently handle and move the pouch as may be required.

The tab may be configured to allow to the pouch to be closed. This feature may preferably be used in combination with a peripheral seal that is re-sealable. Thus, the tab provides a handling point for the user to close the pouch, this can be particularly useful after using the catheter as the rest of the pouch may be dirty or soiled and so is undesirable to touch.

The tab may be any suitable size or shape, such as rectangular, square, circular, elliptical, or irregular in shape. Various shapes and sizes of a tab are discussed below but of course each tab may be the same or different shapes.

The tab may extend from the break-away region, preferably the tab may extend from the centre of an edge of the break-away region. The tab may extend from the base or upper edge of the break-away region. The edge of the break-away region may be slanted towards the tab. The tab may span at least 30%, 40%, 50%, 60%, or 70% of the width of the break-away region. The tab may span no more than 80%, 70%, 60%, 50% or 40% of the width of the break-away region. The tab may have a length that is similar to its width. The tab may have any suitable shape, such as rectangular, triangular or semi-circular. Thus, the tab is easily identifiable at the end of the break-away region.

A tab may be curved. Preferably the tab is curved in a direction away from the plane of the pouch. Thus, the tab may naturally bend away from the pouch which makes it easier to grasp and separate the tab from the pouch. A wall of the pouch may curve away from the tab. Thus the pouch bends away from the tab which also makes it easier to grasp and separate the tab from the pouch.

The tab may comprise a gripping element, for example a gripping hole. The gripping hole may provide a grippy surface or feature. The gripping hole may comprise an aperture through the tab. The gripping hole may be any suitable size or shape, for example, rectangular, square, circular, elliptical. In one embodiment, the gripping hole is in the shape of a stadium, that is a rectangle with semicircles replacing two opposite sides. The parallel sides of the gripping hole may be parallel to the base and top of the tab. Thus, the addition of a gripping hole to a tab allows the user to easily grasp it, of course a hole itself may not be necessary and instead any feature that allows the user to easily grasp the tab could be used.

An edge (e.g. base or upper edge) of the pouch may comprise a gripping hole, for example a gripping hole. The gripping hole of the pouch may have any one or more of the features of the gripping hold of the tab described above. Preferably, the gripping hole of the pouch has the same size/shape as the gripping hole of the tab. The gripping hole of the tab may be in overlap with the gripping hole of the pouch. Thus, the user can more easily separate the pouch and the tab.

The opening may be provided in the pouch by separating the break-away region from the pouch to reveal the access aperture as described above.

The pouch may comprise an internal wall. The internal wall may define the first and second compartments. The first compartment may comprise the rear wall and internal wall. The second compartment may comprise the front wall and internal wall. The internal wall may be the same material as the front wall and or rear wall of the pouch. The internal wall may be fluid impermeable. Thus, the compartments can be simply defined by including an additional wall within the pouch and further the wall prevents or at least inhibits liquid from passing between the compartments.

The internal wall may be arranged to inhibit wetting fluid from the fluid reservoir wetting the second compartment and the fluid collection bag arranged therein. Advantageously, this means that the fluid collection bag remains dry prior to use. Beneficially, for the user, in particular for users with limited dexterity, this means handling and re-packaging of the bag during and after use is considerably easier than if the bag is wetted with wetting fluid. Moreover, this arrangement allows a user to vigorously shake the pouch after wetting fluid is released from the fluid reservoir, therefore, ensuring distribution of wetting fluid to the catheter without the risk of wetting the fluid collection bag. Beneficially, this ensures that there is sufficient wetting fluid to activate the whole catheter surface, therefore, preventing, or at least significantly reducing, discomfort and injury during use.

The internal wall may be attached to the pouch by the peripheral seal. The internal wall may span the entire width of the pouch. The internal wall may span a majority of the height of the pouch, for example at least 50%, 60%, 70%, 80%, or 90% of the height of the pouch, most preferably the internal wall spans 80% of the height of the pouch. The internal wall may extend from the base of the pouch. Each compartment may be planar. The first and second compartment may be arranged parallel to one another. Thus, the internal wall ensures that both the first and second compartments are adequately sized and further the pouch may be sealed with the internal wall within by forming the peripheral seal in a single step.

The internal wall may comprise a separating edge. The separating edge may not form part of the peripheral seal. Access between the first and second compartments may be provided at or adjacent to the separating edge. The separating edge may be a free edge in that it is not sealed to either the front or rear walls of the pouch. In such embodiments, access may be provided between the first and second compartments at all points along the separating edge.

The separating edge may comprise a cut-away region. The cut-away region may be cut into the internal wall/separating edge. The cut-away region may be centrally located across the width of the pouch. The cut-away region may have a size which is substantially equal to, or greater than, the diameter of the catheter. The catheter may be arranged such that before withdrawal of the catheter from the pouch, a portion of the catheter (preferably a portion at or adjacent the distal end) is positioned within the cutaway region. Preferably, the cut-away region may have a size which is substantially equal to, or greater than, the diameter of the catheter tube, and that before withdrawal of the catheter from the pouch, the catheter tube is positioned within the cut-away region. The cut-away region may span at least 10%, 20%, 30%, 40%, 50%, or 60% of the width of the pouch and/or break-away region. The cut-away region may have any suitable shape or size, for example, semi-circular, triangular, rectangular, or irregularly shaped. In one example, the cut away region is trapezoid. The cut-away region may be an inverted (isosceles) trapezoid. The cut-away region may have an aspect ratio (length: width) of 1:2.

Advantageously, this arrangement provides for a connection between the fluid collection bag and the catheter which does not impact the ability of the pouch to retain the wetting fluid in the first compartment. Thus, the fluid collection bag remains dry prior to use. Moreover, typically, a catheter is of sufficient length such that the distal end of the catheter is not required to be inserted into the body during use. Thus, in embodiments where a portion of the distal end of the catheter tube is positioned in the cut-away region, it is not essential for this portion of the catheter to be wetted by the wetting fluid. As such, the catheter tube can be positioned within the cut-away region without having a detrimental effect on the use of the catheter.

The separating edge may be sealed along part of its length to the front or rear wall (preferably rear wall). Thus, access is only provided along a part of the separating edge. Access between the first and second compartments may be provided (solely) by the cut-away region. This can help to control and restrict access between the compartments.

The opening/access aperture may be provided in a wall of the pouch that defines the second compartment, e.g. the front wall. The break-away region may form part of the second compartment. Thus, when the break-away region is separated from the pouch, access to the second compartment is provided.

The catheter may be arranged in the first compartment in any suitable configuration. The catheter may be arranged in a curved/coiled configuration. Thus, the catheter is less likely to suffer damage from kinking etc.

The fluid collection bag may be configured to be withdrawn through the opening before the catheter. The fluid collection bag may be configured to withdraw the catheter from the pouch. Thus, the fluid collection bag facilitates removal of the catheter from the pouch without the user having to touch the catheter.

The fluid collection bag may obscure the catheter from the opening. The fluid collection bag may obscure the rest of the contents of the bag from the opening. Thus, the user is less likely to see and then immediately grasp or touch the catheter itself. The front panel, rear panel and bond between the two panels may define an internal cavity. The internal cavity may be provided with a plurality of internal baffles, as described in relation to the first aspect.

The catheter assembly may comprise a handling element. The handling element may be configured to engage the catheter tube. The handling element may comprise a handling portion mounted to a sleeve. The handling element may be annular. The handling element may be arranged surrounding a portion of the catheter tube. The handling element may be movable along the catheter tube. The handling element may permit gripping of the catheter tube when the handling element is gripped by a user. The handling portion may be arranged around the sleeve. The sleeve extend beyond the handling portion. The sleeve may extend to the side of the handling portion toward the proximal end of the catheter. The sleeve may extend to the side of the handling portion toward the distal end of the catheter.

The handling element may be more rigid than the sleeve. The handling element may be formed of silicon. The handling element may comprise at least one rib to assist gripping by the user. The sleeve may comprise a thermoplastic polyurethane (TPU) or low-density polyethylene (LDPE). Thus, the sleeve is cheap and easy to produce and can be easily manipulated by the user during use.

The sleeve may have a width of at least about 10 mm, about 155 mm, about 20 mm, about 25 mm, about 30 mm, about 35 mm, about 40 mm, about 45 mm, or at least about 50 mm. The sleeve may have a width of no more than about 10 mm, about 155 mm, about 20 mm, about 25 mm, about 30 mm, about 35 mm, about 40 mm, about 45 mm, or no more than about 50 mm.

The sleeve may have a length of at least about 10 mm, about 15 mm, about 20 mm, about 25 mm, about 30 mm, about 35 mm, about 40 mm, about 45 mm, or at least about 50 mm. Each sleeve may have a length of no more than about 10 mm, about 155 mm, about 20 mm, about 25 mm, about 30 mm, about 35 mm, about 40 mm, about 45 mm, or no more than about 50 mm.

The handling portion may have a width of at least about 10 mm, about 15 mm, about 20 mm, about 25 mm, about 30 mm, about 35 mm, about 40 mm, about 45 mm, about 50 mm, about 55 mm, about 60 mm, about 65 mm, about 70 mm, about 75 mm, or at least about 80 mm. The handling portion may have a width of no more than about 10 mm, about 155 mm, about 20 mm, about 25 mm, about 30 mm, about 35 mm, about 40 mm, about 45 mm, about 50 mm, about 55 mm, about 60 mm, about 65 mm, about 70 mm, about 75 mm, or no more than about 80 mm.

The handling portion may have a length of at least about 10 mm, about 15 mm, about 20 mm, about 25 mm, about 30 mm, about 35 mm, about 40 mm, about 45 mm, about 50 mm, about 55 mm, about 60 mm, about 65 mm, about 70 mm, about 75 mm, or at least about 80 mm. The handling portion may have a length of no more than about 10 mm, about 155 mm, about 20 mm, about 25 mm, about 30 mm, about 35 mm, about 40 mm, about 45 mm, about 50 mm, about 55 mm, about 60 mm, about 65 mm, about 70 mm, about 75 mm, or no more than about 80 mm.

Advantageously, the handling element may be used to progressively introduce the proximal end of the catheter into the urethra until fluid flows through the catheter from the bladder.

According to a third aspect of the present invention there is provided a packaged catheter assembly comprising a catheter, a pouch, and a fluid collection bag configured to receive fluid from the catheter in use, wherein: the catheter and fluid collection bag are arranged within the pouch; the pouch comprises an interaction region to form an opening in the pouch and allow the fluid collection bag and catheter to be removed from the pouch; and the fluid collection bag is arranged adjacent to the opening.

With this arrangement, the fluid collection bag protects the catheter from coming into contact with dirt as the pouch is opened and also helps prevent the user from accidentally touching the catheter during opening of the pouch. This helps to reduce risk of infection during use of the pouch as the catheter is less likely to be dirty.

In addition, in embodiments which do not include the two compartments of the second aspect of the invention and where the pouch must be shaken to distribute wetting fluid within it, advantageously the fluid collection bag also reduces the amount of fluid which reaches the opening (which may be at the top of the bag during shaking) and does not otherwise act to wet the surface of the catheter. The fluid collection bag may be any suitable shape or size, for example rectangular, circular, elliptical, cuboid, spherical, etc. The fluid collection bag may comprise two panels: a front panel and a rear panel. The fluid collection bag may comprise a peripheral bond joining the periphery of the front panel and rear panel to form the fluid collection bag. The peripheral bond may define a base, two lateral edges and an upper edge of the fluid collection bag. The two lateral edges may comprise a right lateral edge and a left lateral edge. The right lateral edge and left lateral edge may be defined as the right and left sides of the bag when viewing the bag with the rear panel behind the front panel, the base at the bottom of the bag and the upper edge at the top of the bag. The bag may have a width between the left lateral edge and right lateral edge of at least 10, 12, 15 or 20 cm. The bag may have a width no more than 25, 20, or 15 cm. Preferably, the width is between 10 and 20 cm, most preferably between 12 and 15 cm. The base may define a bottom of the bag. The upper edge may define a top of the bag. The height of the bag from the base to the upper edge may be at least 15, 2025, 30, 35 or 40 cm. The height of the bag may be no more than 45, 40, 35, 30, 25 or 20 cm. The height may be between 20 and 40 cm, 30 and 35 cm, or most preferably 33 and 35 cm. The bag may be configured to hold at least 500, 700, or 1000 ml of fluid, and may hold no more than 1000 ml, for example, it may hold at least 700 ml of fluid.

The peripheral bond may provide a water-tight bond. Preferably, the peripheral bond provides a sterile seal. The peripheral bond may comprise any one or more of: a weld; mechanical seal; heat seal; pressure seal; adhesive; solvent bond; ultraviolet bond; ultrasonic weld; laser weld; impulse weld; or friction weld. This ensures that the catheter is maintained within a sterile environment prior to use and also that once the catheter has been used any fluid contained within the bag does not leak out unintentionally.

The fluid collection bag may be configured to be withdrawn through the opening before the catheter. The fluid collection bag may be configured to withdraw the catheter from the pouch. Thus, the fluid collection bag facilitates removal of the catheter from the pouch without the user having to touch the catheter. The fluid collection bag may be arranged no more than 1 cm, 2 cm, 3 cm, 4 cm, 5 cm, 6 cm, 7 cm, 8 cm, 9 cm, 10 cm, 11 cm, 12 cm, 13 cm, 14 cm or no more than 15 cm from the interaction region. The fluid collection bag may be arranged abutting a seal where the opening is to be formed. Thus, the fluid collection bag is conveniently located against the interaction region where it is easily accessible to the user upon forming the opening in the pouch.

The fluid collection bag may be arranged to span across a majority of the width of the pouch. The fluid collection bag may span at least 50%, 60%, 70%, 80%, or 90% of the width of the pouch, or span at least 50%, 60%, 70%, 80%, or 90% of the opening of the pouch. Thus, the fluid collection bag forms a barrier across the opening in the pouch and protects the contents of the pouch.

The fluid collection bag may be arranged to span across between about 5 and about 80 %, between about 6 and about 70 %, between about 7 and about 60 %, between about 8 and about 50 %, between about 9 and about 45 %, between about 10 and about 40 %, between about 11 and about 35 %, between about 12 and about 30 %, between about 13 and about 25 %, between about 14 and about 20 %, between about 14 and about 18 %, between about 14 and about 16 %, or about 15 % of the length of the pouch.

The fluid collection bag may span at least 5%, 6%, 7%, 8%, 9%, 10%, 12%, 14%, 16%, 18%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 60%, 70%, 80%, or 90% of the length of the pouch. Thus, the fluid collection bag forms a barrier across the opening in the pouch and protects the contents of the pouch.

The fluid collection bag may obscure the catheter from the opening. The fluid collection bag may obscure the rest of the contents of the bag from the opening. Thus, the user is less likely to see and then immediately grasp or touch the catheter itself. This helps to reduce risk of infection during use of the pouch as the catheter is less likely to be dirty, and prevents the user touching wetting fluid on the catheter which can make handling and re-packaging of the fluid collection bag difficult.

The fluid collection bag may be configured to separate the two walls of the pouch. The fluid collection bag may be configured to separate the two walls of the pouch at the opening of the pouch. Thus, once the opening is formed in the pouch, the fluid collection bag removes the need for the user to separate the walls of the pouch which can be inconvenient or difficult, especially for users with reduced mobility.

The fluid collection bag may be arranged to occupy between about 5 and about 50 %, between about 10 and about 45 %, between about 12 and about 40 %, between about 14 and about 35 %, between about 16 and about 30 %, between about 18 and about 25 %, or about 20 % of the internal volume of the pouch.

The fluid collection bag may be arranged to occupy at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, or at least about 70% of the internal volume of the pouch.

The fluid collection bag may be arranged to occupy no more than about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, or no more than about 70% of the internal volume of the pouch.

The inlet of the fluid collection bag may be arranged adjacent to one lateral edge of the pouch. Where the packaged catheter assembly comprises a gripping element and/or a tear start, the inlet of the fluid collection bag may be arranged on the same side of the pouch as the gripping element and/or tear start. Thus, the inlet is positioned to ensure the distal end of the catheter is arranged along the same side of the pouch as the gripping element and/or tear start. This helps the catheter to be withdrawn in a smooth and straight pulling action parallel to the lateral edge of the bag which reduces the force required to remove the catheter from the pouch.

The fluid collection bag may be provided in a stowed configuration. In the stowed configuration, the fluid collection bag may be folded or rolled to reduce its size in any one dimension. The stowed configuration may be a folded or rolled configuration. Thus, the size of the fluid collection bag is minimised inside the pouch and this assists the user in removing the bag and other elements of the packaged catheter assembly from the pouch. The stowed configuration of the fluid collection bag inhibits fluid flow onto the exterior surface of the fluid collection bag as it must penetrate between folds. An axis of the stowed fluid collection bag may be arranged parallel to the tear line of the pouch and/or the opening formed in the pouch. This helps to protect the contents of the pouch from dirt when opening the pouch as the fluid collection bag provides an additional fluid impermeable barrier.

A first end of the stowed fluid collection bag (for example the inlet) may be arranged adjacent to one lateral edge of the pouch, or a first end of the opening. A second end of the stowed fluid collection bag (distal the first end) may be arranged adjacent a second end of the opening. For example, the first end of the stowed fluid collection bag may be arranged adjacent to the tear start. Thus, the fluid collection bag is positioned to ensure the distal end of the catheter is arranged along the same side of the pouch as the tear start. This helps the catheter to be withdrawn in a smooth and straight pulling action parallel to the lateral edge of the bag which reduces the force required to remove the catheter from the pouch.

The catheter may be arranged within the pouch in a curved and/or coiled configuration. The distal end of the catheter may be adjacent to the inner (left or right) lateral edge near the upper edge of the pouch. The catheter may extend down the inside of the pouch. The catheter may extend down through the aperture in the gripping element. The catheter may have a broadly elliptical anti-clockwise (or clockwise) coil as viewed with left lateral edge on the left, and upper edge at the top. The coil may have a single turn around the inner perimeter of the left lateral edge (or right lateral edge), base, and right lateral edge (or left lateral edge) of the pouch. The proximal end of the catheter may rest on the outside of the catheter’s coil. The proximal end of the catheter may rest adjacent to the left lateral edge (or right lateral edge and base of the pouch. Thus, the catheter is safely stored within the pouch in a curved configuration which minimises risk of damage to the catheter - for example through kinking of the catheter - and also facilitates easy withdrawal of the catheter by pulling it by its distal end.

The inlet of the fluid collection bag may be positioned at a comer of the peripheral bond. The fluid collection bag may comprise a neck adjacent to the inlet. The neck may comprise one or more projections extending into the fluid collection bag. The one or more projections may comprise regions of the peripheral bond that extend into the bag. The one or more projections may restrict fluid flow through a region of the bag adjacent to the inlet. The projections may be configured to provide gripping points adjacent to the inlet. Thus, the fluid collection bag resists the flow of fluid back towards the inlet and also is more easily handled by the user.

Any one or more of the one or more projections may have any one or more of the features of a projection as described below.

A projection may have any suitable size or shape. A projection may be triangular, square, rectangular, circular, ellipsoidal or irregularly shaped, preferably, a projection is triangular. A point on the projection furthest from an edge of the bag may be a (right-angled) comer in the projection. The projection may be a right-angled triangle. The hypotenuse of the projection may be aligned parallel to an edge of the bag. Thus, the projections can be suitably shaped to minimise loss of volume in the bag due to the projections. In addition, its shape can help to direct fluid flow within the bag, for example assisting flow into the bag and reducing flow out of the bag.

A projection may extend along no more than 90%, 80%, 70%, 60%, 50%, 40%, 30%, 20% or 10% of the length of an edge of the bag. A projection may extend by at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, or 90% of the length of an edge of the bag. A projection may comprise a comer of the bag. A projection may not comprise from a corner of the bag. Thus, the projections can be flexibly sized and positioned to be most effective.

A projection may be a lateral projection extending from a left (or right) lateral edge of the bag. The lateral projection may be provided on the same side of the bag as the inlet. The lateral projection may extend along 10-40% of the length of the lateral edge of the bag, preferably 25%. The lateral projection may extend across 5-20% of the width of the bag, preferably 10%. The lateral projection may be a right-angled triangle. The right-angled vertex of the lateral projection may project into the bag. The right-angled vertex may be positioned below the inlet inside the bag. The right-angled vertex may be positioned 10% of the way from the upper edge to the base of the bag. The non-right-angled vertices of the lateral projection may be provided on the lateral edge of the bag from which the lateral projection extends. Thus, the lateral projection can assist in directing the flow of fluid into the bag and also helps prevent fluid flowing directly from the bag back up into the sleeve/catheter.

A projection may be an end projection extending from the upper edge or base of the bag. Preferably, the end projection extends from the upper edge. The end projection may be provided adjacent to the inlet. The end projection may extend along 40-95% of the width of the bag, preferably 90%. The end projection may extend from a corner of the bag. The end projection may extend down 5-20% of the length of the bag, preferably 10%. The end projection may be a right-angled triangle. The right- angled vertex of the end projection may project into the bag. The right-angled vertex may be positioned adjacent the inlet inside the bag. The right-angled vertex may be positioned 20% of the way across the width of the bag. The non-right- angled vertices of the lateral projection may be provided on the edge of the bag from which the end projection extends. Thus, the end projection can assist in directing the flow of fluid into the bag and also helps prevent fluid flowing directly from the bag back up into the sleeve/catheter.

In a preferred embodiment, the fluid collection bag comprises both a lateral projection and an end projection extending from the upper edge of the bag as described above. Thus, the two projections work together to assist the user in handling the bag and also to manage fluid flow into/out of the bag.

A projection may comprise a rib. The rib may resist bending or deformation in a given direction. The rib may facilitate folding of the fluid collection bag. The rib may assist the user in grasping or gripping the bag. The strengthening element may comprise a region of the projection that is thicker or thinner than the rest of the projection. The rib may be any suitable shape or size, such as a line which could be straight or curved. The rib may extend across the projection. The rib may extend from an edge of the bag. The rib may extend from a midpoint of the projection along the edge of the bag. The rib may extend to a point on the projection furthest from the edge of the bag, for example a right-angled vertex of a right-angled projection. The rib may be at an angle (i.e. not parallel or perpendicular to) an edge of the bag. Preferably, the lateral projection may comprise a rib. Thus, the mechanical properties of the projection can be controlled through use of a rib to the benefit of the user. A projection may be a join that is independent from the peripheral bond of the fluid collection bag. A join may have any one or more of the features of a projection as described herein. A join can be beneficial to reduce the total area of the panels of the fluid collection bag that are sealed together.

The fluid collection bag may comprise a finger hole. The finger hole may be sized to allow a user to put their finger through the finger hole and handle the bag. Thus the finger hole allows the bag to be handled more easily by a user. The finger hole may be provided at an edge of the bag. The finger hole may be provided in the peripheral bond of the bag. The finger hole may be provided at a comer of the bag. The finger hole may be provided at any of the following comers: where the left lateral edge meets the base; where the base meets the right lateral edge; where the right lateral edge meets the upper edge; or where the upper edge meets the left lateral edge. Where the finger hole is provided in the bag, the peripheral bond may be shaped to accommodate the finger hole. The peripheral bond may truncate a comer of the bag to accommodate the finger hole. The peripheral bond may project into the bag to accommodate the finger hole. As an alternative to the finger hole, the fluid collection bag may comprise a series of ridges or otherwise easily gripped surface or feature in the place of the finger hole to allow the bag to be easily handled.

The fluid collection bag may comprise more than one finger hole, for example at least two, three or more finger holes. One, two, three or more, or each finger hole may have any one or more of the features of the finger hole described above. Thus, easy handling of the bag is facilitated through positioning of finger holes or equivalent features which also does not restrict or affect the volume of liquid that can be contained by the bag.

The finger hole may be provided in a projection of the fluid collection bag. Preferably, the end projection as described above comprises a finger hole. The finger hole may be positioned adjacent to the right-angled vertex of the end projection.

The one or more finger holes may be configured to allow the bag to be rotated to a horizontal position wherein the base of the bag is aligned vertically. In a preferred embodiment, the fluid collection bag comprises a finger hole at either end of the right lateral edge, and/or a finger hole at either end of the left lateral edge, and/or a finger hole along the upper edge and a finger hole along the base. Advantageously, this allows the bag to be rotated in a controlled manner which aids with handling and using the bag.

The fluid collection bag may comprise a fill level indicator. The fill level indicator may comprise fill markers. The fill markers may allow the user to measure the volume of fluid contained within the fluid collection bag. The fill markers may be regularly spaced or irregularly spaced. The fill markers may correspond to an absolute volume of liquid contained within the bag. The fill markers may correspond to a proportion of the volume of the bag which is filled with fluid. The fill markers may indicate when a safe fill level of the bag has been reached. The fill level indicator may be positioned in a transparent or translucent region of the bag. Thus, the fill level indicator ensures the bag is not overfilled.

The pouch may comprise a sheath arranged around the fluid collection bag. The sheath may be configured to inhibit wetting fluid from the fluid reservoir from wetting the exterior of the fluid collection bag.

The pouch may comprise a flexible plastics material. For example, polypropylene (PP), polyethylene terephthalate (PET), low density polyethylene (LDPE), metalized polyester (MET PET) or orientated polypropylene (OPP).

The pouch may comprise two walls (a front wall and a rear wall) and a peripheral seal between the two walls. The peripheral seal may provide a sterile seal. Thus, the pouch may maintain the sterility of its contents.

The peripheral seal may form one or more edges of the pouch, as described in further detail in relation to the second aspect of the invention.

One edge of the pouch may comprise a folded edge. A folded edge may comprise a fold between the two walls. All edges other than the folded edge may be formed by the peripheral seal. The pouch may be formed by folding the two walls to form the folded edge. Thus, the pouch can be flexibly constructed from folding material if required.

The fluid reservoir may be configured to retain wetting fluid within it. The fluid reservoir may be configured to release fluid into the pouch. The pouch may comprise a wetting region in which fluid released by the fluid reservoir preferentially collects. The wetting region may comprise a lower section of the pouch. The wetting region may comprise the bottom 50%, 40%, 30%, 20%, or 10% of the pouch, preferably 20%. Preferably the wetting region is adjacent to the base of the pouch. The pouch may be configured to form a pool of released fluid in the wetting region. Thus, the catheter may be more efficiently wetted by being passed through the pool of wetting fluid formed in the pouch.

The fluid reservoir may be provided as a separate device, or incorporated into the pouch material. The fluid reservoir may comprise a deformable, frangible or burstable sachet. Thus the fluid reservoir is conveniently located within the pouch where it may directly release fluid into pouch to wet the catheter. A deformable, frangible or burstable reservoir enhances the convenience for a user as fluid can be easily released without additional tools and before the pouch is unsealed, thus reducing the chances of accidental wetting of the user. A sachet in particular can be easily handled on an assembly line and introduced more simply than attempting to handle fluid, so as to it into the package during manufacture.

The wetting fluid may activate the surface of the catheter and render it lubricious. The wetting fluid may be water, such as where the catheter has a hydrophilic surface. Any suitable wetting fluid may be used, for example polar (e.g. water-based) or non-polar (e.g. oil-based) wetting fluids depending on the surface properties of the catheter. The fluid reservoir may be configured to retain at least 5, 10, 15, 25, or 50 ml of wetting fluid.

The fluid reservoir may be a sachet. The fluid reservoir may be any suitable shape or size, such as square, rectangular, circular, ellipsoidal or irregularly shaped. Preferably, the fluid reservoir is elongate and rectangular. The fluid reservoir may have a length of at least 60%, 70% or 80% the height of the pouch. The fluid reservoir may have a length no more than 90%, 80% or 70% the height of the pouch. Preferably the fluid reservoir has a length of 80% the height of the pouch. The fluid reservoir may have a width of at least 5%, 10%, 15% or 20% the width of the pouch. The fluid reservoir may have a width of no more than 25%, 20%, 15% or 10% the width of the pouch. Preferably, the fluid reservoir has a width of 15% the width of the pouch. Thus, the fluid reservoir may be flexibly shaped and sized to conveniently fit within the pouch.

The fluid reservoir may be arranged with its length parallel to one edge of the pouch. Preferably, the length of the fluid reservoir is parallel to the left and/or right lateral edge of the pouch. The fluid reservoir may be arranged adjacent to one edge of the pouch. Preferably, the fluid reservoir is arranged adjacent to the same edge of the pouch that the fluid reservoir’s length is parallel to. Thus, the fluid reservoir is conveniently located against an edge of the pouch where it does not take up too much space.

The pouch may be formed from an opaque material. The pouch may have a textured or printed fabric-like appearance and/or feel. Where the pouch is opaque, the pouch may comprise a wetting marker to assist the user in locating the fluid reservoir within the pouch. Thus, the pouch is more comfortable and discreet for the user to carry in day-to-day life and the user can easily find and activate the fluid reservoir.

The opening may be in or near an upper edge, left lateral edge, base or right lateral edge of the pouch. The opening, or a portion of the opening, may be formed at a corner where the upper edge and left lateral edge meet, a corner where the left lateral edge and base meet, a corner where the base and right lateral edge meet, or a comer where the right lateral edge and upper edge meet. The opening may be formed at one or more of these comers and one or more of the edges of the pouch. For example, the opening may be formed at the upper edge and the corner where the upper edge and left lateral edge meet.

The pouch may comprise an interaction region defining a first point of contact for a user of the packaged catheter assembly. The interaction region may facilitate user access to the contents of the pouch. Actuation of the interaction region may create an opening in or near an upper edge of the peripheral seal of the pouch. The catheter may be withdrawn through the opening. Thus, access to the pouch is provided at or near an upper edge of the pouch and as such, the fluid in the pool adjacent the base of the pouch is retained in the pouch while the catheter is withdrawn reducing the risk of spilling fluid outside the pouch. The interaction region may comprise a breakable region of the peripheral seal of the pouch. The method may comprise forming a breakable region in the peripheral seal. The breakable region may comprise a tear-away region which may comprise a tear line defining a line along which the pouch may be tom to at least partially separate the tear-away region from the remainder of the pouch, thereby creating an opening in the peripheral seal. The tear-away region may comprise a tear start. The tear start may be provided at a first end of the tear-away region. The tear start may comprise a notch, or area of weakness, in one or both of the walls of the pouch. The tear start may define the first part of the pouch to be tom. The tear-away region may comprise a tear stop. The tear stop may be provided at a second end of the tear-away region. The tear stop may act to prevent or reduce the likelihood of the tear-away region being completely separated from the remainder of the packaging. A tear line may be defined between the tear start and the tear stop. The tear line may be configured to preferentially tear. The tear line may comprise a weakened region of the pouch. The tear line may be formed by any suitable means, such as laser scoring. Thus the breakable region provides a convenient and easy means to open the pouch with minimal effort and no additional equipment/tools.

The tear-away region may be substantially triangular in shape having a sloped upper edge. The tear-away region may be tapered. The tear-away region may extend upwards more on one side than the other, preferably the tear-away region extends upwards more on the side corresponding to the tear start. The tear-away region may extend upwards no more than 200%, 100%, 75%, or 50% more on one side than the other. The tear-away region may extend upwards at least 25%, 50%, 75%, 100%, or 150% more on one side than the other. Preferably, the tear-away region extends upwards 50% more on one side than the other. Thus, the tear-away region is conveniently shaped to guide the user to grasp it on one side to open the pouch and also provides sufficient material for the user to securely grasp it on that side.

The interaction region may comprise an aperture. The aperture may be sized to allow a finger to pass through and grip the interaction region. Preferably, the aperture is located in the tear-away region. The aperture may be located on the same side of the pouch as the tear start. The aperture may be located adjacent to the tear start. The aperture may be any suitable shape, for example, circular, elliptical, square or irregularly shaped. Preferably, the aperture is circular. Thus, the user can more easily grasp the tear-away region and open the pouch.

The pouch may comprise an opening through which the fluid collection bag may be configured to be withdrawn. The fluid collection bag may be configured to be withdrawn from the pouch before the catheter. The fluid collection bag may be configured to withdraw the catheter from the pouch. Thus, the fluid collection bag facilitates removal of the catheter from the pouch without the user having to touch the catheter.

In a broad aspect, there is provided a catheter assembly comprising a fluid collection bag and a catheter; the fluid collection bag comprising a panel, an inlet to receive fluid from the catheter, and a base, wherein the fluid collection bag is configured to stand up on the base. The fluid collection bag may comprise two panels. The fluid collection bag may comprise a peripheral bond between the two panels. The two panels may be configured to form the base. The base may be distal from the inlet.

Accordingly, a fourth aspect of the present invention provides a catheter assembly comprising a fluid collection bag and a catheter; the fluid collection bag comprising two panels, a peripheral bond between the two panels, and an inlet to receive fluid from the catheter, wherein: the two panels are configured to form a base of the fluid collection bag distal from the inlet; and the fluid collection bag is configured to stand up on the base.

Advantageously, the fluid collection bag is free-standing and is more convenient to use as it does not need to be hung or held during filling. As it is freestanding, with the inlet distal the base, the bag also fills more efficiently with liquid and can ensure that more of the bag is filled with liquid. This means the fluid collection bag can have a smaller form factor which is cheaper, lighter and more discreet for the user.

The fluid collection bag may comprise a base panel. The base panel may span between the front panel and rear panel along the base of the peripheral bond. The base panel may be configured to form a base of the fluid collection bag. That is to say the base of the fluid collection bag may be formed by the front panel, the rear panel and the base panel. The base panel may be configured to allow the front panel and rear panel to separate to form the base of the fluid collection bag. The front panel may be joined to the base panel. The rear panel may be joined to the base panel. The front and rear panels may be joined to opposite sides of the base panel. The base may be formed by two flanges; the rear panel joined to the base panel may form one flange and the front panel joined to the base panel may form the other flange. Consequently, the front panel and rear panel may be (directly) joined by the peripheral bond (only) along an upper edge, left lateral edge and right lateral edge of the fluid collection bag. Thus, the base panel may be used to form a base of the bag and allow it to be free-standing.

The base panel may be elongate. The base panel may comprise two curved edges. The base panel may be lens shaped. The front and rear panel may be joined at the two respective curved edges. The two flanges may extend from the two curved edges. Thus, the base panel is efficiently attached to the fluid collection bag and does not interfere with the lateral edges of the bag.

The base panel may comprise a stowed configuration. In the stowed configuration, the base panel may be configured to reduce the internal volume of the fluid collection bag. The base panel may be folded in the stowed configuration. The base panel may be folded between the front and rear panels. The base panel may be configured to fold to allow the front and rear panels to come together. Thus, the base panel may be folded to allow the fluid collection bag to reduce in size which assists with storage and transport of the bag making it lighter and more discreet for the user.

The base panel may be configured to automatically unfold. The base panel may be configured to unfold as liquid enters the fluid collection bag. Thus, the fluid collection bag can be automatically deployed into a standing configuration as liquid enters the bag, for example under the weight of liquid entering/inside the bag. This makes the bag easier to use as the user does not need to manually unfold it.

The fluid collection bag may comprise an inlet. The inlet may be configured to receive the catheter into the fluid collection bag. The inlet may be configured to prevent the catheter from being (completely) removed from the fluid collection bag, for example separation of the catheter from the fluid collection bag. The inlet may engage with a part of the catheter, preferably the distal end and/or funnel. Thus, fluid can be securely and easily transferred from the catheter into the fluid collection bag and the risk of leaks associated with the separation of the catheter from the fluid collection bag is minimised (through engagement of the inlet and catheter).

The upper edge of the peripheral bond may comprise a neck. The inlet may be located on the neck. The neck may project out in the plane of the fluid collection bag. The neck may project away from the fluid collection bag. The neck may span at least 10%, 20%, 30%, 40%, 50%, 60%, or 70% of the length of the upper edge. The neck may be positioned at any point on the upper edge, but preferably on one side of the upper edge, or in the middle of the upper edge. The neck may be any suitable shape, but preferably it is a truncated triangle, or a triangle. The neck may comprise a left sloped edge and/or a right sloped edge. The left sloped edge and right sloped edge may project from the upper edge and converge at the inlet. Thus, the neck spaces the inlet from the rest of the bag which makes it easier for the user to locate. The provision of a neck can also help liquid entering the bag to be dispersed evenly within the bag.

The fluid collection bag may comprise an outlet to allow fluid to be drained from the bag. The inlet and the outlet may be positioned next to one another. The outlet may be sealed to allow fluid to fill the bag. The outlet may comprise a pull ring configured to be pulled and thereby form an opening in the bag. The pull ring may be configured to be moved in a direction away from the inlet to form the opening. The inlet may be configured to be folded along a neck fold-line. Once folded, the neck foldline may form an edge of the bag. The pull ring may project beyond the edge of the bag defined by the neck fold-line.

Accordingly, a fifth aspect of the present invention provides a fluid collection bag for use with a catheter having a proximal end for insertion into the body and a distal end, the fluid collection bag comprising an inlet to allow fluid to enter the bag from the distal end of the catheter, and an outlet to allow fluid to be drained from the bag, wherein the inlet and the outlet are positioned next to one another, the outlet is sealed to allow fluid to fill the bag, the outlet comprises a pull ring configured to be moved in a direction away from the inlet to form an opening in the bag, and the inlet is configured to be folded so as to form an edge of the bag with the pull ring projecting beyond the edge.

Advantageously, the outlet is sealed so there is a low risk of leakage of fluid during filling the bag. In addition, the folding of the inlet reinforces the bag and inlet to ensure the opening is easily and reliably formed with clean edges that allow controlled emptying of the bag.

The inlet and outlet may be positioned on the same edge of the bag. The inlet may positioned centrally on an edge of the bag. The outlet may be positioned between the neck and a lateral edge of the bag. The outlet may be positioned at a comer of the bag. Thus, tearing/shear forces on the bag are minimised as they are concentrated on the comer of the bag this reduces the likelihood of the bag breaking and spilling liquid.

The fluid collection bag may comprise more than one finger hole, for example at least two, three or more finger holes. One, two, three or more, or each finger hole may have any one or more of the features of the finger hole described above. Thus, easy handling of the bag is facilitated through positioning of finger holes or equivalent features which also does not restrict or affect the volume of liquid that can be contained by the bag. The one or more finger holes may be configured to allow the bag to be rotated to a horizontal position wherein the base of the bag is aligned vertically. In a preferred embodiment, the fluid collection bag comprises a finger hole at either end of the right lateral edge, and/or a finger hole at either end of the left lateral edge, and/or a finger hole along the upper edge and a finger hole along the base. Advantageously, this allows the bag to be rotated in a controlled manner which aids with handling and using the bag.

The outlet may be positioned distal from a finger hole of the bag. Where the outlet is positioned at or adjacent to an edge of the bag, that edge may be free from finger holes. Where the outlet is position at or adjacent an edge of the bag, a different edge of the bag (that is the right/left lateral edge) may comprise one or more finger holes. For example, the outlet may be provided at one corner of the bag and a finger hole may be provided at an opposite comer of the bag. Thus, the finger holes are positioned on edges of the bag that generally do not correspond to the position of the outlet, this makes handling/emptying of the bag easier as the bag can be rotated and held using the finger holes to allow fluid to leave the bag due to gravity.

The outlet may project beyond an upper edge of the bag. The outlet may comprise a spout that projects from the upper edge of the bag. The pull-ring may be attached to the spout. The spout may be any suitable shape, for example rectangular, square, triangular or irregularly shaped, preferably it is rectangular or square. Advantageously, the outlet/spout projects from the edge of the bag and as such is easier to tear off the bag without damaging the rest of the bag and risking uncontrolled release of fluid from the bag.

The pull-ring may be disposed between the spout and inlet. The pull-ring may have any suitable shape, for example circular, elliptical, rectangular, square, triangular, or irregularly shaped. Thus, as the pull-ring is disposed between the spout and the inlet, when it is moved away from the inlet, shearing force from the movement is concentrated at the point the outlet meets the rest of the bag. This facilitates controlled tearing of the bag to create the opening.

The inlet may extend away from the bag, for example where the bag comprises a neck as described above. The outlet and the inlet may extend/project the same distance beyond an edge of the bag. The outlet and inlet/neck may have corresponding shapes. The outlet and inlet/neck may be shaped to fit into, around or next to one another. The pull-ring may be shaped to fit into, around or next to the inlet/neck. As such, there may be little or no gaps between the outlet/pull-ring and inlet/neck. Where the neck is triangular as described above, the pull-ring may also be triangular in shape. The pull-ring may have the shape of a right-angled triangle with two perpendicular sides and a hypotenuse. The hypotenuse may be parallel and/or adjacent to one of the left sloped edge or right sloped edge of the neck. One of the perpendicular sides may form a side of the spout. As the inlet and outlet project the same distance beyond the edge of the pouch and have corresponding shapes, they protect one another from damage due to being caught on other objects.

The outlet may comprise a point of weakness. The point of weakness may be disposed in the peripheral bond at a point the outlet meets the peripheral bond. The point of weakness may be disposed at a point the outlet meets a lateral edge of the peripheral bond. The point of weakness may be arranged at the start and/or end of the opening. The point of weakness may be a notch, or thinned section, in the peripheral bond. The outlet may comprise one or more points of weakness as described above. The outlet may comprise a tear line. The tear line may comprise a weakened region of the outlet. An end of the tear line may comprise a point of weakness. Where the outlet comprises two or more points of weakness, a point of weakness may be positioned at either end of the tear line. The tear line may be configured to preferentially tear. The tear line may be formed by any suitable means, such as laser scoring. Thus, the provision of one or more points of weakness further assist controlled tearing of the bag by providing points in the outlet which preferentially break to form parts of the opening such as the start and/or end.

The fluid collection bag may comprise a retaining element. The retaining element may be configured to receive at least part of the catheter to stow the catheter after use.

According to a sixth aspect of the invention, there is provided a catheter assembly comprising a fluid collection bag and a catheter, the fluid collection bag comprising a retaining element configured to receive at least part of the catheter to stow the catheter after use.

Advantageously, the retaining element ensures the catheter is stowed which makes the catheter assembly more hygienic to store and dispose of after use without having to carry a separate item, such as a bag, to stow/store the catheter in.

The catheter may be configured to be coiled when stowed. Thus, the catheter’s size is minimised to ensure it is stowed efficiently.

The retaining element may be permanently attached to the fluid collection bag. Thus, the retaining element is unlikely to be lost or become separated from the fluid collection bag, this makes it more convenient and easier to use.

The retaining element may comprise a pocket on the outside of the fluid collection bag. The pocket may be configured to receive a majority of the length of the catheter after use. The pocket may comprise a flexible sheet material, for example any one of the materials that were described in relation to the fluid collection bag above. Preferably, the pocket comprises a liquid impermeable material. Thus the pocket prevents liquid passing from the used catheter to the outside of the pocket where it could cause a hygiene risk if it comes into contact with the user or another object.

The pocket may have any suitable shape and size to stow the catheter, for example, the pocket may span the entire width (or length) of the fluid collection bag. In other embodiments, the pocket may not span the entire width (or length) of the fluid collection bag. Preferably, the pocket spans the entire width of the fluid collection bag. Preferably, the pocket spans a majority of the height of the fluid collection bag. The pocket may span 50-80% of the height of the fluid collection bag, for example at least 50%, 60%, or 70% of the height of the fluid collection bag and most preferably 60%. Thus, the pocket can be used to safely store the catheter and prevent inadvertent contact with it by the use.

The pocket may be attached to the fluid collection bag by the peripheral bond. The pocket may be joined to a base of the fluid collection bag. The pocket may be joined to left and/or right lateral edges of the fluid collection bag. Thus, the pocket can be easily attached to the bag in a single step when forming the peripheral bond. The retaining element may comprise a strap. The strap may be configured to seal the catheter against the fluid collection bag after use. The strap may comprise a strip of material. The strap may be configured to seal to the fluid collection bag. The strap may be configured to seal to the catheter. The strap may be configured to seal to itself. The strap may seal to the fluid collection bag/catheter/itself via any suitable adhesive, for example an epoxy resin or alternatively a silicone-based adhesive. The strap may be re-sealable, for example through a resealable adhesive, an additional adhesive that is activated prior or during resealing, or a hook and loop/hook and hook fastener. Thus, the strap can be configured to seal to a variety of different surfaces to ensure the catheter can be easily stowed.

A part of the strap may be permanently attached to the fluid collection bag. For example, a part of the strap may be permanently attached to the fluid collection bag by any one or more of: a weld; mechanical seal; heat seal; pressure seal; adhesive; solvent bond; ultraviolet bond; ultrasonic weld; laser weld; impulse weld; or friction weld. Thus, as part of the strap is attached to the bag it is easier to retain the catheter against the bag. Preferably, one end of the strap (a first end) is attached to the bag. Thus, the rest of the strap can be used most efficiently to stow the catheter.

A part of the strap may be configured to temporarily attach to the fluid collection bag. A part of the strap may be re-sealable. Preferably, one end of the strap is re- sealable. A second end of the strap may be the re- sealable end. Thus, the catheter can be arranged in the stowed configuration and then the strap used to retain it in place by attaching the second end of the strap to the bag. This makes the strap more convenient to use as, for example, the user doesn’t need to feed the catheter through a gap between the strap and bag.

The retaining element may be configured to restrict the size of the fluid collection bag. Thus, the fluid collection bag can be more convenient and discreet for the user to transport, store, use and dispose of. The fluid collection bag may comprise one or more stowed configurations, for example a rolled configuration and/or a folded configuration. The strap may be configured to retain the fluid collection bag in a stowed configuration. A part of the strap (the first end) may be configured to seal to one panel of the fluid collection bag (e.g. the front panel). A different part of the strap (the second end) may be configured to seal to another panel of the fluid collection (e.g. the rear panel). Thus, the strap may retain the fluid collection bag in a folded configuration, which can help control and reduce leaks of liquid out of the bag.

In the folded configuration, the fluid collection bag may comprise a fold (in an upper region of the fluid collection bag, for example adjacent to the upper edge and/or neck). Thus, the passage of liquid towards the inlet from inside the bag is reduced by the fold helping to prevent leaks. The strap may be configured to extend around the fold. Thus, the strap ensures the fold is maintained.

The fluid collection bag may comprise a rolled configuration. The fluid collection bag may be arranged in the rolled configuration prior to use. For example, the fluid collection bag may be provided in the rolled configuration in a sterile sealed pouch. The strap may extend (all the way) around the fluid collection bag in the rolled configuration. The strap may seal to itself when retaining the fluid collection bag in the rolled configuration. Preferably, one end (e.g. the second end) may be configured to seal to another part of the strap. Thus, the fluid collection bag’s size is minimised making it more convenient and discreet to store prior to use.

As mentioned above, the catheter assembly may comprise a pouch and may a packaged catheter assembly. The retaining element may be configured to restrict movement of the fluid collection bag within the pouch, for example, the retaining element may retain the fluid collection bag in a particular part of the pouch. Thus, the fluid collection bag can be more easily accessible to the user when opening the pouch. The retaining element may be configured to (temporarily) attach the fluid collection bag to a part of the pouch, for example a wall of the pouch. The retaining element may be configured to retain the fluid collection bag adjacent to an opening formed in the pouch. Thus, the fluid collection bag is attached to the pouch wall next to the opening which makes it easier to identify and access.

The retaining element may comprise a release mechanism. The release mechanism may be configured to release the retaining element such that the fluid collection bag can be released from the pouch and/or unrolled/unfolded prior to use. The release mechanism may comprise a gripping hole or other tactile element to make it easier to use. Thus, the retaining element can be easily deactivated and the fluid collection bag used.

The release mechanism may comprise a pull-tab. The pull-tab may comprise a tab configured to be pulled by the user to release the retaining element. One end (the second end) of the strap may be the pull-tab. Thus, a tab is easy for the user to grasp and intuitive to use.

The release mechanism may comprise a release marker. The release marker may comprise a logo, marking, a different colour/shade of colour, or different texture/tactile feel than the rest of the fluid collection bag/release mechanism/retaining element. The release marker may be recognisable visually. The release marker may be recognisable through touch. The release marker may be configured to instruct the user how to activate the release mechanism. The release maker may comprise a pullmarker. The pull-marker may be configured to instruct the user to pull the release mechanism/pull-tab in a particular direction, for example, the pull-marker may comprise a directional arrow or point in that direction.

The pouch may comprise one or more side walls, for example two side walls. The side walls may be configured to allow the front and rear walls to separate. Each side wall may comprise a lateral side of the pouch. The side walls may be elongate in a direction parallel to the length of the pouch. The side walls may be triangular, i.e. substantially triangular. The side walls may extend between the front and rear walls of the pouch. The side walls may extend along the left and/or right lateral edge of the pouch. The side walls may not extend along one or more edges of the pouch, for example the base and/or upper edge of the pouch. Thus, the side walls can be used to increase the internal volume of the pouch while minimising the size of the front and rear walls.

The folded edge may be configured to resist being broken. A frangible portion of the peripheral seal may form one or more edges of the pouch that do not comprise the folded edge, in particular, all the edges other than the folded edge may form the frangible portion. The frangible portion may be configured to break before the folded edge. The pouch may comprise only one folded edge. The pouch may contain any one or more of the fluid collection bag and catheter. The fluid collection bag may be provided in a stowed configuration while inside the pouch. Thus, the size of the fluid collection bag is minimised inside the pouch and this assists the user in removing the bag and other elements of the packaged catheter assembly from the pouch.

The catheter assembly may comprise a fluid reservoir. The fluid reservoir may be configured to retain a wetting fluid within it. The fluid reservoir may be configured to release wetting fluid to activate the catheter. The wetting fluid may activate the surface of the catheter and render it lubricious. The wetting fluid may be water, such as where the catheter has a hydrophilic surface. Any suitable wetting fluid may be used, for example polar (e.g. water-based) or non-polar (e.g. oil-based) wetting fluids depending on the surface properties of the catheter. The fluid reservoir may be configured to retain at least 5, 10, 15, 25, or 50 ml of wetting fluid.

The fluid reservoir may be contained within the pouch. The fluid reservoir may be a sachet. The fluid reservoir may be any suitable shape or size, such as square, rectangular, circular, ellipsoidal or irregularly shaped.

The fluid reservoir may be configured to release wetting fluid when activated by a user. The fluid reservoir may be activated by a user by any suitable means, for example twisting the fluid reservoir, or applying a compressive force to the fluid reservoir. The fluid reservoir may be flexible. The fluid reservoir may comprise a flexible plastics material, for example, a thermoplastic polyurethane (TPU) or low- density polyethylene (LDPE). Under application of a compressive force, the fluid reservoir may configured to break when a threshold compressive force is exceeded. The pouch may comprise a wetting marker. The wetting marker may be on a surface of the pouch. The wetting marker may comprise a region of the pouch that is identifiable to the user, for example through visual and/or tactile feedback. Preferably, the wetting marker may be at least visually recognisable, for example a different colour, or pattern, to the pouch. The wetting marker may be the opening marker of the tab as discussed above. Thus, the fluid reservoir does not prematurely release the wetting fluid and the user can easily control the release of wetting fluid by pinching the fluid reservoir between their fingers to break the fluid reservoir and release wetting fluid into the sleeve.

The catheter may comprise a sleeve configured to enclose part of the catheter. Preferably, the sleeve is configured to enclose only part of the length of the catheter. The sleeve may be tubular. The sleeve may comprise a flexible plastics material. The sleeve may comprise perforations about its circumference. The sleeve may comprise a line of weakness (provided by the perforations). The sleeve may be configured to separate into two tubular handling elements. Thus, the sleeve is cheap and easy to produce and can be easily manipulated by the user during use.

The tubular sleeve may be provided in the cut-away region of the internal wall. Thus, the sleeve provides a plug which prevents liquid from inadvertently passing along the outside of the catheter and through the cut-away region into the second compartment during wetting.

The sleeve may comprise a handling element. The handling element may project away from the catheter in a plane parallel to the axis of the catheter.

Thus, according to a seventh aspect of the present invention there is provided a catheter assembly comprising a catheter having a proximal end for insertion into the body and a distal end, and a sleeve configured to enclose only part of the length of the catheter, wherein the sleeve comprises a handling element projecting away from the catheter in a plane parallel to the axis of the catheter.

Advantageously, the provision of a handling element that projects away in a plane parallel to the axis of the catheter is more easy for the user to handle, especially where they have reduced dexterity. The projection of the handling element provides more space on the handling element for assistive features that help the user in manipulating the catheter without touching it. Also, as the handling element needs to only project in one plane, it can be packaged into a 2D packaging without substantially increasing the size of the package.

The handling element may extend in a plane which contains the axis of the catheter. Thus, the handling element extends in a 2D plane from the side of the catheter which means it can be more space efficient while providing direct and intuitive handling of the catheter itself.

The handling element may extend from one side of the catheter. The handling element may extend from only one side of the catheter. Thus, the handling element can allow the user to visualise the position of the catheter more easily as they are only holding it from one side and so the other side is visible.

The handling element may have a thickness measured in a direction perpendicular to the plane in which the handling element extends from the catheter. The thickness of the handling element may be no more than three times, two times or one and a half times the diameter of the catheter. Thus, the handling element does substantially increase the thickness of any packaging required to package the catheter/catheter assembly.

The handling element may have a length in a direction parallel to the axis of the catheter. The length of the handling element may be no more than 8 cm, 7 cm, 6 cm, 5 cm or 4 cm. The length of the handling element may be at least 3 cm, 4 cm, 5 cm, 6 cm or 7 cm. The handling element spans a minority of the length of the catheter. The handling element may be more rigid than the catheter. This helps to ensure that the catheter can be adequately wetted by wetting fluid prior to use and also allows the handling element to be relatively rigid compared to the catheter (which makes for easier handling of the catheter) without excessively restricting the curvature of the catheter. This is beneficial as restriction of the curvature of the catheter can lead to damage due to excessive curvature and kinks in other parts of the catheter.

The handling element may have a width in a direction perpendicular to its thickness and length. The width of the handling element may be at least 1/4, 1/3, or 1/2 the length of the handling element. Consequently, the handling element is planar.

The handling element may comprise a bore through which the catheter extends. A internal diameter of the bore may be at least lx, 1.5x or 2x the diameter of the catheter. The bore may allow the handling element to be moved along the length of the catheter. The bore may be sized to fit over an inlet of the fluid collection bag. Thus, the handling element can be used to manipulate the catheter along its entire length. The handling element may comprise a projection that is the part of the handling element that extends away from the catheter. The projection may be any suitable shape, for example rectangular, triangular, semi-circular or irregularly shaped. Preferably, the projection is rectangular. The projection may have rounded edges. Thus, the handling element is more comfortable for the user to grasp.

The handling element may comprise a gripping element configured to allow the user to grasp the handling element. The gripping element may comprise a gripping hole as described below, or an otherwise easily gripped feature such as a series of ridges or high friction surface. The gripping hole may be any suitable shape, for example, rectangular, square, triangular, circular or elliptical. The gripping hole may be stadium shaped, with its length parallel to the length of the handling element. The gripping hole may be centrally positioned on the projection. The gripping hole may correspond to a majority of the surface of the projection. The projection may define the edges of the gripping hole. Thus, the gripping hole provides the user with a convenient way to handle the catheter via the handling element.

The handling element may be configured to be retained close or at the fluid collection bag/distal end of the catheter. The handling element may engage the inlet of the fluid collection bag and/or distal end of the catheter. The bore may engage the inlet of the fluid collection bag and/or distal end of the catheter. Thus, the handling element can be retained in a position that is easy for the user to grasp and also that ensures the proximal end of the catheter is free from the handling element and is able to be wetted by wetting fluid.

The sleeve may comprise two or more handling elements. Each handling element may comprise the any one or more of the features of the handling element described above. Each handling element may be identical. Each handling element may be different. Preferably, the sleeve comprises two handling elements. Thus, the user has two different handling elements and can therefore do more complex manipulation of the catheter without risking touching the catheter surface directly.

The two or more handling sleeve elements may be joined together. The two or more handling sleeve elements may be temporarily sealed together, for example through a tack weld, temporary adhesive or mechanical fastener such as hook and hook or hook and loop type fasteners. The two or more handling sleeve elements may be configured to be separated. This can provide more control on the position of the handling elements with respect to each other prior to use and make is easier for the user to locate them both.

The two or more handling sleeve elements may be provided separately (and not connected/joined together). Thus, the user does not need to separate them to use them independently, this can be more suitable for users with reduced dexterity or strength.

The handling elements/sleeve may be liquid impermeable. The sleeve may comprise a thermoplastic polyurethane (TPU) or low-density polyethylene (LDPE).

The sleeve/handling element may be provided in the second compartment of the pouch. Thus, the sleeve/handling sleeve element is not likely to be wetted during wetting of the catheter in the first compartment and so is easier and more pleasant for the user to handle.

The catheter assemblies of the first to seventh aspects may include any one or more features of a catheter assembly as defined in general terms, or according to the first to seventh aspects set out above. The catheter assemblies of the first to seventh aspects may comprise any of the optional features of the first to seventh aspects without necessarily including all the features required of them. That is to say, an optional feature which happens to be set out following one particular aspect does not necessarily apply only to that aspect, so, for example, the disclosure provides for the packaged catheter assembly of the second aspect comprising a catheter, a fluid reservoir comprising wetting fluid, and a pouch, wherein: the pouch is divided into first and second compartments; the fluid reservoir and at least a portion of the catheter are arranged in the first compartment; and a fluid collection bag (but not necessarily comprising plurality of internal baffles arranged as diametrically opposed pairs of baffles) is connected to the catheter and is arranged in the second compartment; and the fluid reservoir is configured to release the wetting fluid into the first compartment to wet the catheter; and the pouch comprises an interaction region operable by a user to form an opening in the pouch allowing access to at least the second compartment. According to a eighth aspect of the present invention, there is provided a method of manufacturing a packaged catheter assembly, the method comprising the steps of providing a pouch comprising a fluid reservoir and a fluid collection bag, and arranging a catheter within the pouch, wherein the fluid collection bag comprises a front panel and a rear panel, and a bond between the two panels defining an internal cavity; wherein the cavity is provided with a plurality of internal baffles.

The method of the eighth aspect of the invention may be a method of manufacturing the packaged catheter assembly of the first aspect of the invention, which, of course, may include any optional feature outlined above.

According to an ninth aspect of the present invention there is provided a method of manufacturing a packaged catheter assembly comprising the steps of providing a catheter, a fluid reservoir comprising wetting fluid, a fluid collection bag and a pouch divided into first and second compartments; arranging the fluid reservoir and at least a portion of the catheter in the first compartment; connecting the fluid collection bag to the catheter; and arranging the fluid connection bag in the second compartment; wherein the pouch is configured to provide an opening allowing access to at least the second compartment, and through which the catheter may be withdrawn.

The method may comprise providing an internal join dividing the pouch into the first compartment and the second compartment.

The method may comprise providing a channel in the internal join and optionally arranging a portion of the catheter in the channel.

The method may comprise providing an internal wall in the pouch. The internal wall may divide the pouch into the first and second compartments. The method may comprise sealing a separating edge of the internal wall to a wall (e.g. front or rear) of the pouch. The method may comprise providing a cut-away region in the separating edge. The method may comprise arranging the catheter in the cut-away region.

The method of the ninth aspect of the invention may be a method of manufacturing the packaged catheter assembly of the second aspect of the invention, which, of course, may include any optional feature outlined above. According to a tenth aspect of the present invention there is provided a method of manufacturing a packaged catheter assembly, the method comprising the steps of providing a catheter, a pouch, and a fluid collection bag configured to receive fluid from the catheter in use, arranging the catheter and fluid collection bag within the pouch wherein the pouch comprises an interaction region to form an opening in the pouch and allow the fluid collection bag and catheter to be removed from the pouch, and the fluid collection bag is arranged adjacent to the opening.

The method of the tenth aspect of the invention may be a method of manufacturing the packaged catheter assembly of the third aspect of the invention, which, of course, may include any optional feature outlined above.

The method may comprise arranging the catheter in the pouch and then arranging the fluid collection bag in the pouch. This can ensure the fluid collection bag remains adjacent to the opening.

The method may comprise attaching the catheter to an inlet of the fluid collection bag. The method may comprise arranging the inlet on one side of the fluid collection bag.

According to an eleventh aspect of the present invention there is provided a method of manufacturing a catheter assembly comprising the steps of providing a catheter having a proximal end for insertion into the body and a distal end and forming a fluid collection bag, the fluid collection bag being formed by providing two panels, creating a peripheral bond between the two panels, and providing an inlet in the fluid collection bag to receive fluid from the catheter, wherein: the two panels are configured to form a base of the fluid collection bag distal from the inlet; and the fluid collection bag is configured to stand up on the base.

The method of the eleventh aspect of the invention may be a method of manufacturing the catheter assembly of the fourth aspect of the invention, which, of course, may include any optional feature outlined above.

The method may comprise providing a funnel at the distal end of the catheter. The method may comprise positioning the funnel inside the fluid collection bag. Thus, the funnel may be used to prevent separation of the fluid collection bag and catheter. The method may comprise providing a base panel. The method may comprise joining the base panel to the front and/or rear panels of the fluid collection bag. The method may comprise folding the base panel. The base panel may be folded along a line parallel to a base edge of the front and/or rear panels.

According to a twelfth aspect of the present invention, there is provided a method of manufacturing a fluid collection bag, the method comprising providing a bag, forming an inlet in the bag to allow fluid to enter the bag, and forming a sealed outlet in the bag next to the inlet, wherein the outlet comprises a pull ring configured to be moved in a direction away from the inlet to form an opening in the bag, and the inlet is configured to be folded so as to form an edge of the bag with the pull ring projecting beyond the edge.

The method of the twelfth aspect of the invention may be a method of manufacturing the fluid collection bag of the fifth aspect of the invention, which, of course, may include any optional feature outlined above.

The method may comprise forming a finger hole in the bag. The finger hole may be formed at a point distal from the outlet, for example on a different edge of the bag from the outlet. Thus, the finger hole can be more easily use to handle the bag and direct fluid flow out of the outlet.

The method may comprise providing front and rear panels of the fluid collection bag as described in relation to the first aspect of the invention above. The outlet and/or inlet may be provided integrally with the front and rear panels. The outlet and/or inlet may be formed by sealing the front and rear panels together and creating the peripheral bond. Thus, the inlet and/or outlet and fluid collection bag may be formed in a single step which simplifies manufacture.

The method may comprise forming a point of weakness in the outlet. The method may comprise forming a point of weakness at either side of the outlet. The method may comprise forming a tear line extending from at least one point of weakness in the outlet. The tear line may be formed by laser scoring as described in the second aspect of the invention above. According to a thirteenth aspect of the present invention there is provided a method of manufacturing a catheter assembly the method comprising providing a catheter and a fluid collection bag comprising a retaining element, wherein the retaining element is configured to receive at least part of the catheter to stow the catheter after use.

The method of the thirteenth aspect of the invention may be a method of manufacturing the packaged catheter assembly of the sixth aspect of the invention, which, of course, may include any optional feature outlined above.

According to a fourteenth aspect of the present invention, there is provided a method of manufacturing a catheter assembly, the method comprising providing a catheter having a proximal end for insertion into the body and a distal end, and a sleeve configured to enclose only part of the length of the catheter, wherein the sleeve comprises a handling element projecting away from the catheter in a plane parallel to the axis of the catheter.

The method of the fourteenth aspect of the invention may be a method of manufacturing a catheter assembly of the seventh aspect of the invention, which, of course, may include any optional feature outlined above.

According to a fifteenth aspect of the present invention, there is provided a method of unpacking a packaged catheter assembly, the packaged catheter assembly comprising a pouch, a catheter, and a fluid collection bag configured to receive fluid from the catheter, wherein: the catheter, fluid reservoir and fluid collection bag are arranged within the pouch; and the fluid collection bag comprises a front panel and a rear panel, and a bond between the two panels defining an internal cavity; wherein the cavity is provided with a plurality of internal baffles, the method comprising removing the catheter and fluid collection bag from the pouch.

The method of the fifteenth aspect may further comprise, where the fluid collection bag is in a stowed configuration, unfolding the fluid collection bag.

The method may comprise introducing the catheter by its proximal end into the urethra. The method may comprise allowing fluid to pass out of the body via the catheter. Consequently, the method may be a method of using a packaged catheter assembly.

The method of the fifteenth aspect of the invention may be a method of unpackaging a packaged catheter assembly of the first aspect of the invention, which, of course, may include any optional feature outlined above and may be manufactured according to the eighth aspect of the invention.

According to an sixteenth aspect of the present invention, there is provided a method of unpackaging a packaged catheter assembly, the packaged catheter assembly comprising a catheter, a fluid reservoir comprising wetting fluid, and a pouch, wherein: the pouch is divided into first and second compartments; the fluid reservoir and at least a portion of the catheter are arranged in the first compartment; and a fluid collection bag is connected to the catheter and arranged in the second compartment; the method comprising releasing the wetting fluid into the first compartment so as to wet the catheter arranged therein; forming an opening in the pouch allowing access to at least the second compartment and removing the catheter from the pouch, optionally via the second compartment.

The method of the sixteenth aspect of the invention may be a method of unpackaging a packaged catheter assembly of the second aspect of the invention, which, of course, may include any optional feature outlined above and may be manufactured according to the ninth aspect of the invention.

The method may comprise removing the fluid collection bag from the pouch before removing the catheter.

The method may comprise rupturing/bursting/opening the fluid reservoir within the pouch.

The method may comprise locating the fluid reservoir within the pouch via a window in the pouch and/or a wetting marker disposed on the pouch.

The method may comprise introducing the catheter by its proximal end into the urethra. The method may comprise allowing fluid to pass out of the body via the catheter. Consequently, the method may be a method of using a packaged catheter assembly. According to a seventeenth aspect of the present invention there is provided a method of unpackaging a packaged catheter assembly, the packaged catheter assembly comprising a catheter, a fluid collection bag configured to receive fluid from the catheter in use, and a pouch containing the catheter and fluid collection bag, the method comprising using an interaction region to form an opening in the pouch to allow the catheter and fluid collection bag to be removed from the pouch, wherein the fluid collection bag is arranged adjacent to the opening.

The method of the seventeenth aspect of the invention may be a method of unpackaging a packaged catheter assembly according to the third aspect of the invention and may, of course, include any optional feature outlined above and the packaged catheter assembly may be manufactured according to the tenth aspect of the invention.

The method may comprise withdrawing the fluid collection bag from the pouch before the catheter. The method may comprise withdrawing the catheter from the pouch using the fluid collection bag.

The method may comprise unfolding the fluid collection bag. The method may comprise handling the fluid collection bag via one or more projections and/or one or more finger holes disposed on the fluid collection bag.

The method may comprise measuring the fluid contained in the fluid collection bag via a fill level indicator disposed on the fluid collection bag.

According to a eighteenth aspect of the present invention there is provided a method of preparing a catheter assembly for use, the catheter assembly comprising a catheter and the fluid collection bag, the fluid collection bag comprising two panels, a peripheral bond between the two panels, and an inlet to receive fluid from the catheter, the method comprising using the two panels to form a base of the fluid collection bag distal from the inlet; and standing the fluid collection bag up on the base. The method of eighteenth aspect of the present invention may be a method of preparing the catheter assembly of the fourth aspect of the invention, which, of course, may include any optional feature outlined above and may be manufactured according to the eleventh aspect of the invention.

The method may comprise separating the two panels to form the base. The method may comprise unfolding a base panel of the fluid collection bag. The method may comprise introducing liquid into the fluid collection bag. The method may comprise introducing liquid into the fluid collection bag to automatically form the base in the fluid collection bag.

The method may comprise introducing the catheter by its proximal end into the urethra. The method may comprise allowing fluid to pass from the body and into the fluid collection bag via the catheter. Consequently, the method may be a method of using a catheter assembly.

According to a nineteenth aspect of the present invention there is provided a method of draining a fluid collection bag, the fluid collection bag comprising an inlet and a sealed outlet next to one another, the outlet comprising a pull ring, the method comprising folding the inlet to form an edge of the bag with the pull ring projecting beyond the edge, moving the pull ring in a direction away from the inlet to form an opening in the bag, and emptying the contents of the bag out through the opening.

The method of the nineteenth aspect of the invention may be a method of draining a fluid collection bag of the fifth aspect of the invention, which, of course, may include any optional feature outlined above and may be manufactured according to the twelfth aspect of the invention.

The method may comprise forming an opening extending from at least one point of weakness disposed on the outlet. The method may comprise forming an opening along a weakened region of the outlet. Thus, the opening is easily formed in a controlled manner.

The method may comprise rotating the bag such that the outlet is at a point above the rest of the bag, and then forming an opening in the bag. Thus, fluid in the bag is not near the outlet as it is opened which reduces the likelihood of spillage. The method may comprise rotating the bag such that the outlet is at a point below the rest of the bag after forming an opening in the bag. Thus, fluid may flow out of the bag and the bag may be efficiently drained.

The method may comprise rotating the bag by grasping one or more finger holes (disposed at the edges of the bag). The method may comprise grasping a finger hole disposed on an edge of the bag distal from the outlet. Thus, the bag can be rotated in a controlled manner using the finger holes and while reducing the risk of spillages from the outlet.

The method may comprise providing a catheter and introducing the catheter by its proximal end into the urethra. The method may comprise allowing fluid to pass from the body and into the fluid collection bag via the inlet and catheter. Fluid may pass from the catheter into the bag before an opening is formed in the bag with the outlet. Consequently, the method may be a method of using a catheter assembly.

According to a twentieth aspect of the present invention there is provided a method of stowing a catheter assembly after use, the catheter assembly comprising a catheter and a fluid collection bag comprising a retaining element, the method comprising using the retaining element to receive at least part of the catheter and stow the catheter after use.

The method of the twentieth aspect of the invention may be a method of stowing a catheter assembly of the sixth aspect of the invention, which, of course, may include any optional feature outlined above and may be manufactured according to the thirteenth aspect of the invention.

The method may comprise coiling the catheter in order to stow it. The method may comprise arranging the catheter against the fluid collection bag. The method may comprise retaining the catheter against the fluid collection bag and using the retaining element.

The method may comprise folding an upper region of the fluid collection bag. The method may comprise retaining the fluid collection bag in a folded configuration using the retaining element. The method may comprise introducing the catheter by its proximal end into the urethra. The method may comprise allowing fluid to pass out of the body via the catheter. Consequently, the method may be a method of using a catheter assembly.

According to a twenty-first aspect of the present invention, there is provided a method of handling a catheter assembly, the catheter assembly comprising a catheter having a proximal end for insertion into the body and a distal end, and a sleeve configured to enclose only part of the length of the catheter, wherein the sleeve comprises a handling element projecting away from the catheter in a plane parallel to the axis of the catheter, the method comprising grasping the handling element.

The method of the twenty-first aspect of the invention may be a method of handling the catheter assembly of the seventh aspect of the invention, which, of course, may include any optional feature outlined above and may be manufactured according to the fourteenth aspect of the invention.

The method may comprise grasping a gripping hole of the handling element.

The method may comprise separating two or more handling elements. The method may comprise moving the two or more handling elements independently of one another.

The method may comprise introducing the catheter by its proximal end into the urethra. The method may comprise allowing fluid to pass from the body through the catheter. Consequently, the method may be a method of using a catheter assembly.

The methods of the eighth to twenty-first aspects of the present invention may of course individually include any one or more of the features, optional or otherwise, of one another and further may include any one or more of the features, optional or otherwise, of the first to seventh aspects of the present invention.

In any aspect, the catheter assembly is preferably a closed catheter assembly, that is that the catheter assembly comprises a catheter coupled to a fluid collection bag, such that it is configured to collect and retain fluid released from the body through the catheter. The fluid collected/catheter assembly may then be disposed of by the user when is convenient. Of course, embodiments of the invention may also be open catheter assemblies in that fluid is not collected or retained by the catheter assembly. Likewise in any aspect the catheter is preferably a urinary catheter; and/or is an intermittent catheter. Thus, the features of aspects of the present invention allow intermittent male urinary catheters to be adequately wetted prior to use which can be more difficult than for other types of catheter which are generally shorter.

As used herein, ranges and amounts can be expressed as “about” a particular value or range. About also includes the exact amount. For example, “about 5 mm” means “about 5 mm” and also “5 mm.” Generally, the term “about” includes an amount that would be expected to be within experimental error. The term “about” includes values that are within 5% less to 5% greater of the value provided. For example, “about 30mm” means “between 28.5mm and 31.5mm.

Detailed Description of the Invention

In order that the invention may be more clearly understood one or more embodiments thereof will now be described, by way of example only, with reference to the accompanying drawings, of which:

Figure 1 is a front view of a first embodiment of a packaged catheter assembly;

Figure 2 is a cut-away front view of the packaged catheter assembly of Figure 1;

Figure 3 is a front view of the packaged catheter assembly of Figure 1 during withdrawal of the catheter assembly from the pouch;

Figure 4 is a cut-away front view of the fluid collection bag of the packaged catheter assembly of Figure 1 where the catheter assembly has been removed from the pouch and the fluid collection bag is in an open configuration; and

Figure 5 is a partial cut-away front view of the fluid collection bag of Figure 4 after use.

Figure 6 is a front view of a second embodiment of a packaged catheter assembly where the pouch is in the closed configuration;

Figure 7 is a cross-sectional view of the packaged catheter assembly of Figure 6; 3

Figure 8 is a front view of the packaged catheter assembly of Figure 6 where the pouch is in the open configuration and the fluid collection bag has been removed from the pouch;

Figure 9 is a front view of the fluid collection bag of the packaged catheter assembly of Figure 6;

Figure 10 is a front view of fluid collection bag of the packaged catheter assembly of Figure 6 where the neck has been folded;

Figure 11 is a front view fluid collection bag of the packaged catheter assembly of Figure 6 where the outlet has been partially opened;

Figure 12 is a front view of fluid collection bag of the packaged catheter assembly of Figure 6 where the outlet has been completely opened;

Figure 13 is a perspective view of a third embodiment of a packaged catheter assembly where the pouch is in the closed configuration;

Figure 14 is a perspective view of the packaged catheter assembly of Figure 13 where the pouch is in the open configuration;

Figure 15 is a front view of the catheter and fluid collection bag of the packaged catheter assembly of Figure 13; and

Figure 16 is a front perspective view of the fluid collection bag of the packaged catheter assembly of Figure 13 after use.

Referring to Figures 1-3, a first embodiment of a packaged catheter assembly 100 is shown.

The packaged catheter assembly 100 comprises a pouch 170 containing a fluid collection bag 110, a catheter tube, or “catheter” 120, and a fluid reservoir 140 comprising wetting fluid. The catheter 120 has a proximal end 121 for insertion into the body and a distal end 122, and the fluid collection bag 110 is attached to the distal end 122 of the catheter 120 and is arranged to receive fluid from the distal end 122 of the catheter 120, thereby forming a so-called “closed catheter assembly”.

The distal end 122 of the catheter 120 is attached to an inlet 150 of the fluid collection bag 110 via a connector 122a. In this embodiment, the catheter 120 is a male urinary catheter made from a hydrophilic thermoplastic elastomer (TPE). Obviously those skilled in the art will be able to select suitable alternative materials.

In this embodiment, the catheter 120 comprises a handling element 190 comprising a handling portion 191 mounted to a sleeve 192, arranged around the sleeve, such that the sleeve 192, rather than the handling portion 191 is in contact with the surface of the catheter. The handling element 190 is arranged surrounding a portion of the catheter tube 120 and is movable along the catheter tube 120. Two ends 192a, 192b of the sleeve extend either side of the handling portion 191. The first end 192a is arranged on the side of the handling portion 191 toward the proximal end 121 of the catheter 120, and the second end 192b is arranged on the side of the handling portion 191 toward the distal end 122 of the catheter 120.

The first end 192a and the second end 192b of the sleeve each have a width of 28 mm and extend beyond the handling portion 191 by a length of 35 mm. The handling portion 191 has a width of 40mm and a length of 30 mm. Obviously those skilled in the art will appreciate that the handling element is optional, that alternative handling elements could be provided and that these dimensions are merely preferred.

The handling portion 191 is formed of silicon, but clearly those skilled in the art will be able to select suitable alternative materials. The handling element 191 comprises several ribs to assist gripping by the user. The handling element 190 facilitates handling of the catheter 120 by the user. In use, the handling portion 191 can be gripped by a user to exert pressure upon the catheter tube 120 such that the handling element 190 no longer moves along the catheter tube 120 but instead can be used to guide the catheter 120. In use, handling element 133 may be used to progressively introduce the proximal end 121 of the catheter 120 into the urethra until fluid flows through the catheter 120 from the bladder.

The pouch 170 is formed from a front wall 173 and rear wall 171 of identical shape and size, and a peripheral seal joining the periphery of the walls to form the pouch 170 and containing its contents (i.e. the closed catheter assembly and fluid reservoir 140). The peripheral seal defines a base 172a, a left lateral edge 172b, a right lateral edge 172c and an upper edge 172d of the pouch 170. The left lateral edge 172b and right lateral edge 172c being defined as the left and right sides of the pouch 170 when viewing the pouch 170 with the rear wall 171 behind the front wall, the base 172a at the bottom of the pouch 170 and the upper edge 172d at the top of the pouch 170. The peripheral seal thus defines a pouch 170 that is generally rectangular and suitably has a width between the lateral edges of between 100-150 mm, preferably 120-140 mm, for example about 136mm, and a height from the base 172a to the upper edge 172d of between 100 to 250 mm, preferably 150 to 200 mm, for example about 174 mm. The base 172a defines the bottom of the pouch 170 in use, and the upper edge 172d the top. However, in other embodiments alternative shapes and sizes could be conceived, such as elliptical or circular walls forming correspondingly shaped pouches, or even a tubular pouch or pouch with more than two walls, e.g. a prism or other polygon.

The peripheral seal may be formed from any suitable bonding/sealing methods such as chemical adhesives, chemical bonding, ultrasonic bonding, or mechanical bonding. In alternative embodiments, the pouch 170 may be formed from a single piece of material. The pouch may then be formed by folding this single piece of material along a pouch fold line to form the walls. In addition, in some embodiments any number of folds may be used to form the pouch 170. For example, none of the edges may comprise a fold, one edge may comprise a fold, or two or more of the edges may comprise a fold.

In this embodiment, the pouch 170 is formed from an opaque material and as such provides a discrete package for its contents which can make the user more comfortable in carrying the packaged catheter assembly 100 in day-to-day life. In addition, the exterior of the pouch 170 may have a textured or printed appearance, for example a matte appearance, and feel to reduce the impression that it is a medical device.

In this embodiment, the pouch 170 also comprises an interaction region. The interaction region forms the right side of the pouch 170 and spans between the base 172a and upper edge 172d. The interaction region is used to provide access to the pouch through/near to the right lateral edge 172c. In this embodiment, the interaction region comprises a tear-away region 175. The tear-away region 175 comprises a tear start 176 at the point the upper edge 172d meets the tear-away region 175, a tear stop 177 at a corresponding point on the base 172a, and a tear line 178 spanning between the tear start 176 and tear stop 177. The tear line 178 comprises a line of weakness in the walls of the pouch 170, which may be formed by any suitable means but in this embodiment is laser etched. The tear start 176 comprises a notch to provide an area of weakness in the peripheral seal. This allows the tear-away region 175 to be separated from the pouch 170 by tearing the walls apart from the tear start 176 to the tear stop 177 along the tear line 178, therefore, providing access to the contents of the pouch 170. In other embodiments, the tear stop 177 may comprise a small aperture in the walls to prevent further tearing of the pouch 170.

The upper part of the tear-away region 175 comprises a circular aperture 179 sized to allow a finger to pass through and grip the tear-away region 175. To ensure the pouch 170 is fully sealed, the front wall and rear wall 171 are sealed to one another over the entire tear-away region 175. In other embodiments, other seals such as a ziplock arrangement, or hook and hook, hook and loop (VELCRO (RTM)) or the like may be used to provide access to the pouch (or to reseal the pouch after opening), and of course, the sizes and shapes set out above are exemplary.

In this embodiment, the pouch 170 is divided into a first compartment 180a and a second compartment 180b. The compartments 180a, 180b are separated by an internal join 185. The internal join 185 joins the front wall 173 to the rear wall 171 to form a fluid tight seal therebetween. The internal join 185 is a linear, elongated join comprising a first end 185a and a second end 185b. In other embodiments, the internal join 185 may be curved, for example an ‘S’-shape or a ‘U’-shape. The internal join 185 extends toward the interaction region from its first end 185a at the peripheral seal at a comer where the upper edge 172d and the left lateral edge 172b meet. The internal join 185 terminates, at its second end 185b, approximately mid-way between the base 172a and upper edge 172d of the peripheral seal proximal to the right lateral edge 172c of the pouch 170. The second end 185b is separated from the right lateral edge 172c by a channel 195. At the channel 195, the front wall 173 is not joined to the rear wall 171. Unless obstructed, as described below, fluid may pass from the first compartment 180a to the second compartment 180b, and vice versa, via the channel 195. The internal join 185 has a length of approximately 14 cm and a width of approximately 0.8 cm, which is substantially equal to the width of the peripheral seal. The channel 195 has a diameter defined by the distance between the second end 185b of the internal join 185 and the inner perimeter of the right lateral edge 172c. In this embodiment, the channel 195 has a diameter of approximately 0.5 cm which is substantially equal to the diameter of the catheter tube 120 which, in this embodiment, has a diameter classified as CH14 by the French Scale system.

The first end 185a of the internal join 185 is joined to the peripheral seal, therefore, forming a fluid tight seal between the first end 185a of the internal join 185 and the peripheral seal. In other embodiments, the internal join 185 may extend from any part of the peripheral seal, preferably from an edge other than that where the interaction region is provided, and most preferably from the edge opposite to the interaction region. In further embodiments, the first end 185a of the internal join 185 may not be joined to the peripheral seal so as to form a channel between the first end 185a of the internal join 185 and the peripheral seal.

As shown in Figure 2, which shows the embodiment before use, the catheter tube 120 is positioned with the distal end 122 of the catheter 120 in the channel 195, therefore providing a fluid-tight, or at least substantially fluid-tight, seal between the second end 185b of the internal join 185, the catheter 120 and the right lateral edge 172c. In other embodiments, the channel 195 may have a diameter substantially equal to the diameter of connector 122a, or other component, arranged on the catheter 120, and in this embodiment, the connector 122a, or other component, may be arranged in the channel 195.

The first compartment 180a is trapezoidal. The first compartment 180a is bordered by the left lateral edge 172b, base 172a, a portion of, in this embodiment, approximately half the length of, the right lateral edge 172c and the internal join 185. The first compartment 180a comprises the fluid reservoir 140, a significant portion of the catheter tube 120, including its proximal end 121, and the handling element 190.

The second compartment 180b is triangular. The second compartment 180b is bordered by the upper edge 172d, internal join 185, and a portion of, in this embodiment, approximately half the length of, the right lateral edge 172c. The second compartment 180b comprises the fluid collection bag 110, a portion of the distal end 122 of the catheter and the connector 122a, which is connected to the inlet 150 of the fluid collection bag 110.

The arrangement of this embodiment creates a ‘wet region’, upon release of the wetting fluid, as defined by the first compartment 180a, and a ‘dry region’ as defined by the second compartment 180b.

As such, upon release of wetting fluid from the fluid reservoir 140, all of the wetting fluid, or at least a substantial amount, is retained in the first compartment 180a and does not, therefore, contact the fluid collection bag 110. Thus, the fluid collection bag 110 remains dry, therefore, facilitating handling and re-packaging of the bag 110 during and after use.

The internal join 185 may be formed in the same way as the peripheral seal, i.e., from any suitable bonding/sealing methods such as chemical adhesives, chemical bonding, ultrasonic bonding, or mechanical bonding. In the present embodiment, the internal join 185 is formed by plastic welding.

In this embodiment, the catheter 120 is resiliently biased into a straight configuration to the extent that over a distance equivalent to the distance between the channel 195 and base 172a, the catheter 120 resists being bent by more than about 20 degrees. As such, due to the restriction of the tangent of the catheter 120 imposed by the channel 195 and the resilience of the catheter 120 itself, the catheter 120 extends away from the channel 195 substantially parallel to the right lateral edge 172c of the pouch 170 and extends down into the first compartment 180a and adjacent to the base 172a of the pouch 170.

The catheter 120 is arranged within the pouch 170 in a curved and coiled configuration, with the distal end 122 adjacent to the right lateral edge 172c approximately mid-way between the upper edge 172d and the base 172a. The catheter 120 extends down through the first compartment 180a inside of the pouch 170 and into a broadly elliptical clockwise coil (as viewed with left lateral edge 172b on the left, and upper edge 172d at the top). The coil has a single turn around the inner perimeter of the right lateral edge 172c, base 172a, and left lateral edge 172b of the pouch 170, with 9 the proximal end 121 of the catheter 120 resting on the fluid reservoir 140, adjacent to the right lateral edge 172c and base 172a of the pouch 170. Of course, the catheter uncoils as it is pulled out of the pouch, as described below.

In this embodiment, the fluid collection bag 110 is provided in a stowed configuration, which in this embodiment is a folded configuration, within the pouch 170.

In this embodiment, the folded fluid collection bag 110 is arranged within the pouch 170 in the second compartment 180b. The inlet 150 of the bag 110 receives the distal end 122 of the catheter 120 adjacent to the right lateral edge 172c of the pouch 170. The fluid collection bag 110 is therefore arranged adjacent to the opening formed in the pouch 170 by the tear-away region 175 as described further below and spans between the upper edge 172d, internal join 185 and a portion of the right lateral edge 172c.

In this embodiment, prior to use, the handling element 190 is arranged around a portion of the catheter 120 between the inlet 150 and proximal end 121. The distal end 122 of the catheter 120 is positioned in the channel 195. Consequently, only a minority of the length of the catheter 120 is positioned in the channel 195.

In this embodiment, the fluid reservoir 140 is an elongate rectangular burstable sachet of water. The fluid reservoir 140 is arranged within the first compartment 180a of the pouch 170. The fluid reservoir 140 has a height equal to between 60-90% the height of the pouch 170, for example 80%, and a width between 5-25% the width of the pouch 170, for example 15%. In other embodiments, many other types of reservoir would be suitable including different shapes and sizes of reservoir, or non-burstable reservoirs and other external sources of fluid. In this embodiment, the wetting fluid is water and interacts with the hydrophilic surface of the catheter 120 to render it lubricious. In other embodiments, other wetting fluids may be used and they may be polar (e.g. water-based) or non-polar (e.g. oil-based) depending on the catheter’s surface properties.

Referring to Figures 4 and 5, the fluid collection bag 110 comprises a front panel (not shown), a rear panel 110a of identical shape and size, and a peripheral bond joining the periphery of the panels to form the bag 110. The fluid collection bag 110 defines an internal cavity 155. The internal cavity 155 provides the volume of the fluid collection bag 110 which can be filled with liquid during use. The front panel and rear panel 110a are both transparent or translucent in this embodiment. The peripheral bond defines a base 112, a right lateral edge 113, an upper edge 115a, a right neck edge 113a, an uppermost edge 115, a left neck edge 114a and a left lateral edge 114. The right neck edge 113a, uppermost edge 115 and left neck edge 114a define a neck 151 which extends from the left lateral edge 114 and upper edge 115a.

The upper edge 115a extends linearly inwardly at an approximate right angle from the top of the right lateral edge 113. The upper edge 115a extends linearly inwardly approximately 50% of the width of the bag 110.

The right lateral edge 113 and left lateral edge 114 being defined as the right and left sides of the bag 110 when viewing the bag 110 with the rear panel 110a behind the front panel, the base 112 at the bottom of the bag 110 and the uppermost edge 115 at the top of the bag 110. The peripheral bond thus defines a bag 110 that, when unfolded (i.e., in an open configuration), is generally rectangular and suitably has a width between the lateral edges of at least 10, 12, 15 or 20 cm. The bag may have a width no more than 25, 20, or 15 cm. Preferably, the width is between 10 and 20 cm, more preferably between 14 and 19 cm, and most preferably about 17 cm. A height from the base 112 to the uppermost edge 115 may be at least 25, 30, 35 or 40 cm. The height of the bag may be no more than 45, 40, 35 or 30 cm. The height may be between 25 and 45 cm, between 30 and 40 cm, more preferably between 34 and 38 cm, or most preferably about 36 cm. The bag may be configured to hold at least 500, 700, or 1000 ml of fluid, and may hold no more than 1000 ml. For example, it may hold at least 700 ml of fluid. The base 112 defines the bottom of the bag 110 in use, and the uppermost edge 115 the top. However, in other embodiments alternative shapes and sizes could be conceived, such as elliptical or circular panels forming correspondingly shaped bags, or even a tubular bag or bag with more than two panels, e.g. a prism or other polygon.

In this embodiment, the panels comprise a flexible plastics material formed of polypropylene (PP). In this embodiment, the uppermost edge 115 comprises a spout 150a extending upwardly from the uppermost edge 115. At the end of the spout 150a, distal to the fluid collection bag, there is provided an inlet 150 for receiving a catheter tube 120. The spout 150a extends upwardly from the uppermost edge 115 at approximately mid-way between the corner where the left neck edge 114a and uppermost edge 115 meet and the corner where the right neck edge 113a and uppermost edge 115 meet. The spout 150a tapers inwardly as it extends away from the uppermost edge 115. The spout 150a has a length, i.e., the distance from where the spout joins the uppermost edge 115 to the inlet 150, of between 2 and 14 cm, between 4 and 12 cm, between 6 and 10 cm, between 7 and 9 cm, or about 8 cm.

At the base of the neck 151 is a left edge projection 117a and a right edge projection 117b which define the narrowest point of the neck 151. Left edge projection 117a is diametrically opposed to the right edge projection 117b, and each project inwardly at approximate right angles relative to the left lateral edge 114 and right neck edge 113a, respectively. The right edge projection 117b projects inwardly from the comer of where the right neck edge 113a and upper edge 115a meet. The left edge projection 117a projects inwardly from the top of the left lateral edge 114, which is approximately three quarters the height of the bag 110, and is just below the left neck edge 114a. The left edge projection 117a and right edge projection 117b each project inwardly approximately one quarter of the width of the neck 151. Thus the narrowest point of the neck 151 has a width equal to approximately 50% of the distance from the left lateral edge 114a to the right lateral edge 113a.

In this embodiment, the fluid collection bag 110 further comprises a finger hole 116 to allow the bag 110 to be easily handled by a user. The finger hole 116 is arranged to accommodate at least one of the user’s fingers. The finger hole 116 is positioned adjacent to the neck portion 151 and comprises a loop of material attached to the bag 110 at the corner where the uppermost edge 115 and right neck edge 113a meet, and separately at the comer where the right lateral edge 113 and upper edge 115a meet. The loop of material comprises two portions; a transverse part 116a and a lateral part 116b. The transverse part 116a extends, parallel to the upper edge 115a, from the outer perimeter of the corner where the uppermost edge 115 and the right neck edge 113a meet. Thus, the distance from the base 112 to the transverse part 116a is equal to the distance from the base 112 to the uppermost edge 115.

The lateral part 116b extends, parallel to the right neck edge 113a, from the outer perimeter of the corner where the right lateral edge 113 and the upper edge 115a meet. Thus, the distance from the left neck edge 114a to the lateral part 116b is equal to the distance from the left lateral edge 114 to the right lateral edge 113.

In other embodiments, the finger holes 116 may comprise a series of ridges, or otherwise easily gripped surface or feature to allow the user to easily handle the bag 110. In addition, there may be different numbers of finger holes 116, such as two or more than two, and they may be placed in different locations on the bag 110.

The fluid collection bag 110 comprises four internal baffles; first baffle 119a, second baffle 119b, third baffle 119c and fourth baffle 119d.

Each internal baffle 119a, 119b, 119c,l 19d is an elongated join joining the front panel (not shown) to the rear panel 110a. Each baffle 119a, 119b, 119c,119d is provided as a weld. Each internal baffle 119a, 119b, 119c,119d provides a fluid tight seal between the front panel (not shown) and the rear panel 110a.

First internal baffle 119a and second internal baffle 119b each extend linearly inwardly at substantially 90° from the left lateral edge 114. Third internal baffle 119c and fourth internal baffle 119d each extend linearly inwardly at substantially 90° from the right lateral edge 113.

First internal baffle 119a extends inwardly from the left lateral edge 114 at approximately 25% of the distance from the base 112 to the uppermost edge 115.

Second internal baffle 119b extends inwardly from the left lateral edge 114 at approximately 50% of the distance from the base 112 to the uppermost edge 115.

Third internal baffle 119c extends inwardly from the right lateral edge 113 at approximately 25% of the distance from the base 112 to the uppermost edge 115.

Fourth internal baffle 119d extends inwardly from the right lateral edge 113 at approximately 50% of the distance from the base 112 to the uppermost edge 115. As such, first internal baffle 119a and third internal baffle 119c are arranged as a diametrically opposed pair of baffles, and the second internal baffle 119b and fourth internal baffle 119d are arranged as a diametrically opposed pair of baffles.

First internal baffle 119a and second internal baffle 119b each extend inwardly from the left lateral edge 114 a distance equal to approximately 40% of the distance between the left lateral edge 114 and the right lateral edge 113.

Third internal baffle 119c and fourth internal baffle 119d each extend inwardly from the right lateral edge 113 a distance of approximately 40% of the distance between the right lateral edge 113 and the left lateral edge 114.

Thus, each baffle 119a, 119b, 119c, 119d has a length of about 40 % of the width of the fluid collection bag 110.

Diametrically opposed pair of baffles 119a and 119c, therefore, form a first channel 119e between the terminus of each of the first internal baffle 119a and the third internal baffle 119c.

Diametrically opposed pair of baffles 119b and 119d, therefore, form a second channel 119f between the terminus of each of the second internal baffle 119b and the fourth internal baffle 119d.

The diameter of each channel 119e, 119f is equal to about 20% of the width of the fluid collection bag 110. Each channel 119e, 119f is arranged centrally relative to the width of the fluid collection bag 110.

Because each baffle 119a, 119b, 119c, 119d provides a fluid tight seal between the front panel (not shown) and the rear panel 110a, the channels 119e, 119f direct the flow of liquid 125 entering the fluid collection bag 110 via inlet 150 then spout 150a through the internal cavity 155 toward the base of the bag 110. Thus, providing an improved flow of liquid 125 through the fluid collection bag 110, therefore, facilitating filling of the bag 110. The liquid 125 entering the fluid collection bag 110 therefore settles at the base of the bag, which advantageously means that the entire volume of the bag can be filled with liquid 125, thus preventing, or at least significantly reducing, the possibility of the bag 110 overflowing with liquid 125 during use which can be embarrassing for the user. More importantly, when partially filled, the baffles prevent fluid from sloshing about in the bag, or at least reduce the quantity of fluid free to slosh and the space to slosh in - for example when, as shown in figure 5 the space beneath the first and third baffles 119a, 119c is full and the space between the first and third baffles 119a, 119c and the second and fourth baffles 119b, 119d is only partially full, the fluid in the bottom part beneath the first and third baffles 119a, 119c will not slosh around and the fluid above those baffles 119a, 119c will be constrained from sloshing too much by the second and fourth baffles 119b, 119d.

In this embodiment, the fluid collection bag 110 also comprises an interaction region. The interaction region forms the base of the neck 151 of the fluid collection bag 110 and spans between the left neck edge 114a and right neck edge 113a. The interaction region is used to provide access to the fluid collection bag and/or to dispose of its contents more easily near the uppermost edge 115. In this embodiment, the interaction region comprises a tear-away region 275. The tear-away region 275 comprises a tear start 276 at the point the left neck edge 114a meets the tear-away region 275, a tear stop 277 at a corresponding point on the right neck edge 113a, and a tear line (not shown) spanning between the tear start 276 and tear stop 277. The tear line comprises a line of weakness in the panels of the fluid collection bag 110, which may be formed by any suitable means but in this embodiment is laser scored. The tear start 276 comprises a notch to provide an area of weakness in the peripheral bond. This allows the tear-away region 275 and the neck 151 to be partially or fully separated from the fluid collection bag 110 by tearing the panels apart from the tear start 276 to the tear stop 277 along the tear line, therefore, providing access to the contents of the fluid collection bag 110, and/or allowing the contents of the bag 110 to be poured away with greater ease than if the contents were to be poured away through the considerably narrower inlet 150. In other embodiments, the tear stop 277 may comprise a small aperture in the panels to prevent further tearing of the fluid collection bag 110.

The tear-away region 275 comprises a gripping tab 279 sized to allow a finger and thumb to grip the tear-away region 275. After use, when a user requires access to the contents of the fluid collection bag 110, or wants to discard the contents, the gripping tab 279 can be gripped and pulled across the front panel of the fluid collection bag 110 in a direction substantially toward the tear stop 277. This action will separate the neck 151 from the rest of the fluid collection bag 110 and therefore create an opening in the fluid collection bag 110 through which the contents of the bag 110 can be accessed or easily discarded.

To ensure the fluid collection bag 110 is fully sealed, the front panel and rear panel 110a are sealed to one another over the entire tear-away region 275.

In this embodiment, the packaged catheter assembly 100 is provided with the first compartment 180a containing the catheter 120, handling element 190 and fluid reservoir 140, and the second compartment 180b containing the fluid collection bag 110 and a portion of the catheter 120, all contained within the pouch 170 as mentioned above. To wet the catheter 120 so that it is ready for use, the user may release the wetting fluid from the fluid reservoir 140 into the pouch 170. This may be done by any suitable means, but preferably by applying pressure to the outside of the pouch 170 at a region corresponding to the position of the fluid reservoir 140. In this embodiment, the pouch comprises a wetting marker 182 to assist the user in locating the fluid reservoir 140.

In this embodiment, the fluid reservoir 140 is configured to rupture/burst under external pressure, creating a tear (not shown) in the fluid reservoir 140 which releases wetting fluid (not shown) into the first compartment 180a of the pouch 170 where it collects to form a pool in the first compartment 180a of the pouch 170. The pouch can then be shaken gently, ideally whilst held upright, to wet the catheter 120.

The user may then access the catheter 120 by creating an opening in the pouch 170 using the interaction region. The aperture 179 is grasped in one hand, and the pouch 170 below the tear line 178 in another, and the tear-away region 175 is torn from the tear start 176 toward the tear stop 177 along the tear line 178. Thus, the pouch 170 is torn between the upper edge 172d and base 172a, as such, an opening is formed in the pouch 170 that may be used to access its contents. Typically the pouch will be turned on its side, such that the side where the tera away region is formed is uppermost, before opening to avoid wetting fluid spilling out of the pouch. In this embodiment, as shown in Figure 3, the tear-away region 175 is fully separated from the pouch 170 to improve access to the contents of the pouch 170. In other embodiments, the tear-away region 175 may not be fully separated from the pouch 170 to reduce the number of separate parts and make the pouch 170 easier to handle. Moreover, in another embodiment, the tear-away region 175 may be separated to an approximate mid-point between the upper edge 172d and the base 172a, i.e., approximately half the length of the right lateral edge 172c, adjacent to the channel 195. Thus, closed catheter assembly (i.e. catheter 120 and fluid collection bag 110) are accessible to the user via the second compartment 180b but the opening does not extend to the first compartment, therefore, preventing spilling out of the wetting fluid in the first compartment. Other embodiments may also feature other ways to access the pouch for example a zip-lock seal.

In this embodiment, prior to withdrawal, only parts of the catheter 120 that are intended to enter the body should be wetted by the wetting fluid. To ensure that the fluid collection bag 110 is not wetted, the fluid collection bag 110 is arranged in a separate compartment to that of the catheter 120. As described above, in this embodiment this is achieved by the internal join 185 joining the front wall 173 to the rear wall 171 to form a fluid tight seal therebetween, and, therefore, forming a first compartment 180a comprising the catheter 120 and the fluid reservoir 140, and a second compartment 180b comprising the fluid collection bag 110, connector 122a and a portion of the catheter 120. Removal of the catheter assembly from the pouch 170, while keeping the fluid collection bag 110 dry, is facilitated by providing a channel 195 between the second end 185b of the internal join 185 and the right lateral edge 172c of the pouch 170, in which can be positioned the distal end 122 of the catheter 120 joined to the fluid collection bag 110, as described above.

Moreover, providing a channel 195 having a diameter which is substantially equal to the diameter of the catheter 120 inhibits ingress of wetting fluid into the second compartment 180b from the first compartment 180a after rupturing the fluid reservoir 140 and shaking the pouch 170 to distribute the wetting fluid to activate the surface of the catheter 120. Because the fluid collection bag 110 can be withdrawn from the pouch 170 before the wetted catheter 120, the user does not need to touch the wetted catheter 120 before touching the fluid collection bag 110. As such, the user can withdraw the fluid collection bag 110 from the second compartment 180b by partially separating the tear-away region 175 from the remainder of the pouch 170 to a point along the right lateral edge 172c approximately mid-way between the upper edge 172d and the base 172a, thereby creating an opening in the peripheral seal which provides the user with access to the components in the second compartment 180b, i.e. the fluid collection bag 110. By withdrawing the fluid collection bag 110, which is connected to the catheter 120, the catheter 120 is also withdrawn from the pouch 170. Thus, the fluid collection bag 110 remains dry, or at least substantially dry, before and during use. The fluid collection bag 110 may then be unfolded so that it is ready to accept fluid from the catheter 120.

The catheter 120 is now ready for use. The handling element 190 may be used to progressively introduce the proximal end 121 of the catheter 120 into the urethra until fluid flows through the catheter 120 from the bladder. Fluid flowing through the catheter 120 is collected in the fluid collection bag 110. After use, in this embodiment, the catheter 120 is withdrawn from the body and the contents of the fluid collection bag 110 may then be disposed of.

Referring to Figures 6-12, a second embodiment of a packaged catheter assembly 1000 is shown and shares many features with the first embodiment, as such like numerals are used to denote like features.

The assembly 1000 comprises a fluid collection bag 1010, a catheter 1020, a sleeve 1030, a fluid reservoir 1040 and a pouch 1070 containing the fluid collection bag 1010, catheter 1020, sleeve 1030 and fluid reservoir 1040. The catheter 1020 has a proximal end 1021 for insertion into the body and a distal end 1022, and the fluid collection bag 1010 is arranged to receive fluid from the distal end 1022 of the catheter 1020.

In this embodiment, the catheter 1020 is a male urinary catheter made from a hydrophilic thermoplastic elastomer (TPE). Obviously those skilled in the art will be able to select suitable alternative examples.

The pouch 1070 is formed from a front wall 1071a and rear wall 1071b of identical shape and size, and a peripheral seal joining the periphery of the walls to form the pouch 1070 and containing its contents (i.e. the closed catheter assembly and fluid reservoir 140). The peripheral seal defines a base 1072a, a left lateral edge 1072b, a right lateral edge 1072c and an upper edge 1072d of the pouch 1070. The left lateral edge 1072b and right lateral edge 1072c being defined as the left and right sides of the pouch 1700 when viewing the pouch 1070 with the rear wall 1071b behind the front wall 1071a, the base 1072a at the bottom of the pouch 1070 and the upper edge 1072d at the top of the pouch 1070. The peripheral seal thus defines a pouch 1070 that is generally rectangular and suitably has a width between the lateral edges of between 60-110 mm, preferably 90-110 mm, for example about 100mm, and a height from the base 1072a to the upper edge 1072d of between 100 to 250 mm, preferably 120 to 140 mm, for example about 130 mm. The base 1072a defines the bottom of the pouch 1070 in use, and the upper edge 1072d the top. However, in other embodiments alternative shapes and sizes could be conceived, such as elliptical or circular walls forming correspondingly shaped pouches, or even a tubular pouch or pouch with more than two walls, e.g. a prism or other polygon.

The peripheral seal may be formed from any suitable bonding/sealing methods such as chemical adhesives, chemical bonding, ultrasonic bonding, or mechanical bonding. In alternative embodiments, the pouch 1070 may be formed from a single piece of material. The pouch may then be formed by folding this single piece of material along a pouch fold line to form the walls. In addition, in some embodiments any number of folds may be used to form the pouch 1070. For example, none of the edges may comprise a fold (as in the illustrated example), one edge may comprise a fold, or two or more of the edges may comprise a fold.

In this embodiment, the pouch 1070 is formed from an opaque material and as such provides a discrete package for its contents which can make the user more comfortable in carrying the packaged catheter assembly 1000 in day-to-day life. In addition, the exterior of the pouch 1070 may have a textured or printed appearance, for example a matte appearance, and feel to reduce the impression that it is a medical device.

In this embodiment, the pouch 1070 also comprises an interaction region which forms a majority of the front wall 1071a of the pouch 1070. The interaction region is used to provide access to the pouch through/near to the upper edge 1072d. In this embodiment, the interaction region comprises a rectangular break-away region, in the form of a peel-away region 1074. The peel-away region 1074 comprises a base 1074a, left lateral edge 1074b, right lateral edge 1074c and upper edge 1074d that correspond to the base 1072a, left lateral edge 1072b, right lateral edge 1072c and upper edge 1072d of the pouch 1070 respectively. Consequently, the peel-away region 1074 comprises a width between its left lateral edge 1074b and right lateral edge 1074c and a height between its base 1074a and upper edge 1074d. The width of the peel-away region 1074 is between 50-100%, 70-90% or most preferably 80-90% of the width of the pouch 1070, for example 85% of the width of the pouch 1070. The height of the peel-away region 1074 is between 50-100%, 60-90% or most preferably 70-80% of the height of the pouch 1070, for example 75% of the height of the pouch 1070. In this embodiment, the peel-away region 1074 is positioned centrally with respect to the width and height of the pouch 1070.

In this embodiment, the comers of the peel-away region 1074 are rounded to provide a smoother and less jagged appearance to the peel-away region 1074. In other embodiments, the comers may not be rounded.

In other embodiments, the tear-away region may have a different shape or size as required by the shape/size of the pouch 1070 or the contents of the pouch 1070. It may also not be positioned centrally with respect to the width and/or height of the pouch 1070, for example it may be positioned closer to one edge of the pouch than another.

In this embodiment, the peel-away region 1074 is formed from the same material as the front wall 1071a of the pouch 1070 but is a different shade of colour to the front wall 1071a, this gives the pouch 1070 a more continuous feel but makes the peel-away region visually recognisable to the user. In other embodiments, the breakaway region may be formed of a different material.

In this embodiment, the front wall 1071a of the pouch 1070 comprises an access aperture 1078a in a position corresponding to the peel-away region 1074. Around a periphery 1078b of the aperture 1078a, the peel-away region 1074 is attached to the front wall 1071a of the pouch 1070 by a frangible adhesive. This allows the user to form an opening in the pouch 1070 by peeling the peel-away region 1074 away from the front wall 1071a and breaking the frangible adhesive positioned at the periphery 1078b of the aperture 1078a.

In other embodiments the break-away region may be attached to the front wall by any suitable bonding/sealing method, for example chemical adhesives, chemical bonding, ultrasonic bonding, or mechanical bonding, such as hook-and-hook or hook- and-loop fasteners. Alternatively, the break-away region may be formed from the same piece of material as the front wall 1071a. In such (tear-away) embodiments, a line of weakness or tear-line in the front wall may define the tear-away region and allow the user to form an opening in the pouch by separating the tear-away region from the front wall.

In this embodiment, the base 1074a of the peel-away region 1074 is configured not to separate from the front wall 1071a, this prevents the peel-away region 1074 from separating from the pouch 1070 and reduces the number of items that the user must worry about during use of the catheter assembly 1000. In other embodiments, the break-away region may be configured to fully separate from the pouch 1070 - for example to allow for easier access to the contents of the pouch 1070.

In this embodiment, the peel-away region 1074 comprises a front opening tab 1075. The front opening tab 1075 projects from the upper edge 1074d of the peel-away region 1074. The front opening tab 1075 is rectangular in shape with rounded corners and has a width that spans approximately 50% of the width of the upper edge 1074d. The front opening tab 1075 has a height that is approximately half its width

In this embodiment, the front opening tab 1075 is not adhered to the front wall 1071a of the pouch 1070. The front opening tab 1075 in this embodiment is curved away from the plane of the pouch 1070. This makes it easier for a user to grasp the front opening tab 1075 and consequently the peel-away region 1074.

In this embodiment, the tab 1075 overlaps the upper edge 1072d of the pouch 1070. The upper edge 1072d extends beyond the lateral edges of the front tab 1075 as upper edge 1072d extends across the full width of the pouch 1070 whereas the front tab 1075 does not. This helps the user to identify the tab 1075 and separate it from the pouch 1070. The tab 1075 and upper edge 1072d of the pouch 1070 also each comprise a gripping element in the form of a gripping hole 1077. Each gripping hole 1077 of this particular example is in the shape of a stadium, that is a rectangle with semicircles replacing two opposite sides. The parallel sides of each gripping hole 1077 are parallel to the upper edge 1072d of the pouch 1070 and form apertures which allow the user to easily grasp the tab 1075 and pouch 1070. Of course alternative shapes of gripping hole can be readily imagined.

As described above, the tab 1075 allows the user to handle the catheter assembly 1000 more easily and provides a gripping point to allow the user to open the pouch 1070 by separating the peel-away region 1074 from the pouch 1070. The gripping holes 1077 can also be used to hang the catheter assembly 1000 for example when displayed in a shop for purchase.

In this embodiment, the pouch 1070 comprises a first compartment 1081 and a second compartment 1082 separated by an internal wall 1083. The internal wall 1083 comprises a fluid impermeable material that is the same as the material of the front wall 1071a and rear wall 1071b. The internal wall 1083 spans the entire width of the pouch 1070 from the left lateral edge 1072b to the right lateral edge 1072c. The internal wall 1083 spans from the base 1072a of the pouch 1070 up approximately 70-90% of the height of the pouch 1070 and most preferably 80% of the height of the pouch 1070. Consequently, an upper (separating) edge 1084 of the internal wall 1083 is revealed when the peel-away region 1074 is at least partially removed from the pouch 1070. The internal wall 1083 is sealed to the pouch 1070 by the peripheral seal which, in this embodiment, seals together the front wall 1071a, internal wall 1083 and rear wall 1071b.

In this embodiment, the first compartment is defined by the rear wall 1071b and internal wall 1083, and the second compartment is defined by the internal wall 1083 and the front wall 1071a. Thus, the first and second compartments 1081, 1082 comprise two parallel and planar compartments with access provided between them adjacent to the upper edge 1072d of the pouch 1070.

In this embodiment, the internal wall 1083 comprises a cut-away region 1085 cut into the upper edge 1084 of the internal wall 1083. The cut-away region 1085 is centrally located across the width of the pouch 1070 and spans approximately 50% of the width of the peel-away region 1074. The cut-away region 1085 has an inverted isosceles trapezoid shape with a height approximately half its width and legs at either end angled at approximately 70 degrees with respect to the upper edge 1084 of the internal wall 1083. The cut-away region 1085 thereby allows for easier access between the first compartment 1081 and second compartment 1082 towards the centre of the upper edge 1084 of the internal wall 1083. Of course, in other embodiments the cutaway region 1085 may have any suitable shape, such as rectangular, triangular, circular, semi-circular, ellipsoidal or irregularly shaped.

In this embodiment, the fluid reservoir 1040 is configured to retain a wetting fluid and release wetting fluid to activate the surface of the catheter 1020. In this embodiment, the wetting fluid is water and interacts with the hydrophilic surface of the catheter 1020 to render it lubricious. In other embodiments, other wetting fluids may be used and they may be polar (e.g. water-based) or non-polar (e.g. oil-based) depending on the catheter’s surface properties.

In this embodiment, the fluid reservoir 1040 comprises a burstable rectangular sachet positioned within the first compartment 1081 of the pouch 1070 adjacent to the base 1072a of the pouch 1070. The user can release wetting fluid held by the fluid reservoir 1040 by compressing the fluid reservoir 1040, for example by pinching it between their fingers. The user can advantageously do this while the fluid reservoir 1040 is contained within the pouch 1070 as described in more detail below. To facilitate the user in activating the fluid reservoir 1040, the pouch 1070 comprises a wetting marker 1042. The wetting marker 1042 comprises a region of the pouch 1070 that is a different colour or texture to the rest of the pouch 1070 to allow the user to easily identify the position of the fluid reservoir 1040 and where to press to activate it and release wetting fluid into the pouch 1070. In this embodiment, the wetting marker 1042 is disposed on the peel-away region 1074. In other embodiments, the fluid reservoir 1040 may be configured to release wetting fluid through a different means, for example by twisting or bursting the fluid reservoir in a different way.

In this embodiment, the fluid collection bag 1010 comprises a front panel 1011, a rear panel of identical shape and size (not shown), and a peripheral bond joining the periphery of the panels to form the bag 1010. The peripheral bond defines a base 1012, a right lateral edge 1013, a left lateral edge 1014 and an upper edge 1015. The right lateral edge 1013 and left lateral edge 1014 being defined as the right and left sides of the bag 1010 when viewing the bag 1010 with the rear panel behind the front panel 1011, the base 1012 at the bottom of the bag 1010 and the upper edge 1015 at the top of the bag 1010. The peripheral bond thus defines a bag 1010 that is generally rectangular and suitably has a width between the lateral edges of between 10 and 20 cm, and most preferably between 12 and 15 cm, and a height from the base 1012 to the upper edge 1015 of between 25 and 40 cm, 30 and 35 cm, or most preferably 33 and 35 cm. The bag 1010 is thus configured to hold at least 700 ml of fluid released from the user through the catheter safely. The base 1012 defines the bottom of the bag 1010 in use, and the upper edge 1015 the top. However, in other embodiments alternative shapes and sizes could be conceived, such as elliptical or circular panels forming correspondingly shaped bags, or even a tubular bag or bag with more than two panels, e.g. a prism or other polygon.

In this embodiment, the panels comprise a flexible plastics material, for example polypropylene (PP), polyethylene terephthalate (PET), low density polyethylene (LDPE), metalized polyester (MET PET) orientated polypropylene (OPP), polyvinylpyrrolidone (PVP), or polyvinyl chloride (PVC).

In this embodiment, the corners of the peripheral bond at either end of the left lateral edge 1014 each comprise finger holes 1016 to allow the bag 1010 to be easily handled by a user. Where the left lateral edge 1014 meets the base 1012, the peripheral bond truncates the corner of the bag 1010 to accommodate the finger hole 1016, and where the left lateral edge 1014 meets the upper edge 1015, the peripheral bond forms a square projecting into the interior of the bag 1010 with the finger hole 1016 at its centre. In other embodiments, the finger holes 1016 may comprise a series of ridges, or otherwise easily gripped surface or feature to allow the user to easily handle the bag 1010. In addition, there may be different numbers of finger holes 1016, such as only one or more than two, and they may be placed in different locations on the bag 1010.

In this embodiment, the upper edge 1015 of peripheral bond comprises a neck 1050 which spans the middle 50% of the length of the upper edge 1015. In other embodiments, it may be located a different point on the upper edge 1015 or peripheral bond, such as on the left or right lateral edges 1014, 1013, or base 1012, and may have a different size in relation to the rest of the bag 1000 or edge in which it is situated. The neck 1050 projects out from the plane of the bag 1010. The neck 1050 is triangular and comprises a left sloped edge 1051 and a right sloped edge 1052 which project from the upper edge 1015 and converge at an inlet 1053. The inlet 1053 is connected to the catheter 1020 and is configured to received fluid from the catheter 1020 as described below.

In this embodiment, the upper edge 1015 also comprises an outlet 1060 arranged between the neck 1050 and the right lateral edge 1013. The outlet 1060 comprises a rectangular spout 1061 that projects from the upper edge 1015 the same distance as the inlet 1053. The outlet 1060 also comprises a pull-ring 1062 attached to the spout 1061 and disposed between the spout 1061 and neck 1050. The pull-ring 1062 has the shape of a right-angled triangle, with two perpendicular sides and a hypotenuse 1063. The hypotenuse 1063 is parallel and adjacent to the right sloped edge 1052 of the neck 1050. In other embodiments, the pull-ring 1062 may be any suitable shape or size - such as circular, rectangular or square. This helps to protect the neck 1050, inlet 1053 and outlet 1060 as they project out from the fluid collection bag 1010 together without significant gaps between them.

The outlet 1060 also comprises a point of weakness, which in this embodiment is a notch 1064 in the peripheral bond at the point where the spout 1061 meets the right lateral edge 1013. This helps ensure that the opening 1016 is formed cleanly and does not propagate down the right lateral edge 1013 of the pouch. In other embodiments, the outlet may comprise a tear line which comprises a weakened region of the outlet 1016. The notch 1064 may be positioned at an end of the tear line and as such, the tear line further assists with forming the opening 1016. The tear line may be formed by any suitable means, such as laser scoring.

In this embodiment, the fluid collection bag 1010 also comprises a retaining element in the form of a pocket 1017. The pocket 1017 is configured to receive all or part of the length of the catheter 1020 in order to stow the catheter 1020 after use. The pocket 1017 comprises a flexible sheet material, for example, the same material as is used to construct the front/rear panels of the fluid collection bag 1010. The pocket 1017 spans the entire width of the fluid collection bag 1010 and extends from the base 1012 of the bag 1010 up approximately 50-80% of the height of the bag 1010, for example 60% of the height. Thus, the catheter 1020 (and optionally also the sleeve 1030) can be stowed in the pocket 1017 after use, for example using the sleeve 1030. Advantageously, this reduces the likelihood of the user touching the catheter 1020 directly which may be unhygienic and also makes the used catheter 1020 easier to dispose of.

In this embodiment, the distal end 1022 of the catheter 1020 is in fluid communication with the bag 1010 via the inlet 1053.

In this embodiment, the fluid collection bag 1010 is provided in a stowed folded configuration and in a different compartment as the fluid reservoir 1040, consequently, the fluid collection bag 1010 is provided in the second compartment 1082. The inlet 1053 is positioned closer to the cut-away region 1085 and upper edge 1084 of the internal wall 1083 than the rest of the stowed fluid collection bag 1010 and the catheter 1020 extends from the inlet 1053 between the upper edge 1084 of the internal wall 1083 and upper edge 1072d of the pouch 1070 into the first compartment 1081.

The position and configuration of the catheter 1020 in the first compartment 1081 is not particularly limited so long as it is not curved to the extent that damage to the catheter is likely, for example from kinking. In this embodiment, the catheter 1020 is arranged within the first compartment 1081 in a curved/coiled configuration, this helps ensure that the catheter 1020 is not excessively curved and minimises risk of damage.

In this embodiment, the sleeve 1030 comprises two identical handling elements 1031. Each handling element 1031 comprises a bore along its length through which the catheter 1020 extends and which allows the handling element 1031 to be moved along the length of the catheter 1020. Each handling element 1031 is approximately 2- 8 cm in length, preferably 3-7 cm, for example 5 cm in length. Consequently, each handling element 1031 and both handling elements 1031 together span a minority of the length of the catheter 1020. This leaves the majority of the catheter 1020 uncovered and as such easily wetted by wetting fluid released from the fluid reservoir 1040 as described below.

In this embodiment, each handling element 1031 projects away from the catheter 1020 in a plane parallel to the axis of the catheter 1020, and in a plane through which the catheter 1020 extends. In this embodiment, each handling element projects away in only one direction. Each handling element 1031 comprises a planar and rectangular projection 1032 with rounded edges distal from the catheter 1020. Each handling element 1031 comprises a width in a direction perpendicular to its length (and thickness, see below) and parallel to the direction in which it extends from the catheter 1020). The width of each handling element is about 1/2 the length of each handling element. This allows each handling element 1031 to be more easily grasped by the user and used to move and handle the catheter 1020 without touching the catheter 1020 directly. Of course, in other embodiments, each handling element 1031 may project away from the catheter 1020 in multiple directions and may have a different shape such as circular or ellipsoidal.

In this embodiment, each handling element 1031 has a thickness measured in a direction perpendicular to the direction in which each handling element 1031 extends from the catheter 1020. Each handling element has a thickness that is no more than 2x (twice) the diameter of the catheter 1020. This ensures the handline elements 1031 have a low profile and do not cause the packaging/pouch 1070 to be unnecessarily bulky.

In this embodiment, each handling element 1031 comprises a gripping element in the form of a gripping hole 1037 that is stadium shaped like the gripping hole 1077 provided in the opening tab 1075. Each gripping hole 1037 is positioned centrally within the projection 1032 of each handling element 1031 and corresponds to almost the entire surface area of the projection 1032 such that the projection 1032 is simply defining the edges of the gripping hole 1077. Of course, in other embodiments, the gripping hole 1077 may be replaced with any suitable feature that allows the handling element 1031 to be handled more easily, for example a series of ridges.

In this embodiment, each handling element 1031 is independent of the other and is not adhered or sealed to the other. This allows the handling elements 1031 to be easily moved along the catheter 1020 as required by the user. In other embodiments, the handling elements 1031 may be sealed together, this can allow them to more securely remain in a given position prior to use. The user may then separate the handling elements 1031 by breaking a temporary seal that is present between them, for example a tack weld.

While in this embodiment the sleeve 1030 comprises two handling elements 1031, in other embodiments, the sleeve 1030 may comprise a single handling element 1031 or more than two handling elements 1031 as required.

In this embodiment, the handling elements 1031 are arranged on the catheter 1020 adjacent to the fluid collection bag 1010. The bore through each handling element 1031 is sized such that the handling element 1031 can overlie a portion of the inlet 1053 and consequently the handling element 1031 closest to the fluid collection bag 1010 may be push-fit over the inlet 1053 to retain it in place close to the fluid collection bag 1010 before use.

In this embodiment, both handling elements 1031 are located in the second compartment 1082 along with the fluid collection bag 1010. As described above, the fluid reservoir 1040 is arranged in the first compartment 1081 and the catheter 1020 extends from the fluid collection bag 1010 into the first compartment 1081.

Prior to use, the pouch 1070 is provided sealed closed with the contents arranged within it as mentioned above. To ensure the catheter 1020 is wetted prior to use, the user must activate the fluid reservoir 1040 by locating it within the pouch 1070 and squeezing it to rupture the fluid reservoir 1040 and release wetting fluid into the first compartment 1081. This can be done with the aid of the wetting marker 1042 on the outside of the pouch 1070.

Advantageously, once wetting fluid is released into the first compartment 1081 it is prevented from reaching the fluid collection bag 1010 and sleeve 1030 by the internal wall 1083. This ensures that the wetting fluid is most efficiently used to wet the catheter 1020, the majority of which is in the first compartment including the proximal end 1021 of the catheter. In addition, it ensures that the fluid collection bag 1010 and sleeve 1030 remain dry and easier to handle. Once the catheter 1020 has been wetted, the contents of the pouch 1070 can be accessed by opening the pouch 1070. The pouch 1070 is opened by separating the front opening tab 1075 from the pouch 1070 to break the adhesive present around the periphery 1078b of the access aperture 1078a present in the front wall 1071a of the pouch 1070. As the tab 1075 is separated from the pouch 1070, the peel-away region 1074 peels away from the front wall 1071a of the pouch 1070 revealing the contents of the second compartment 1082.

Once the pouch 1070 has been opened, which in some embodiments may involve completely removing the peel-away region 1074 from the pouch 1070, the fluid collection bag 1010, catheter 1020 and sleeve 1030 may be removed from the pouch 1070. Preferably, the user grasps the dry folded stowed fluid collection bag 1010 and/or one or both dry handling elements 1031 of the sleeve 1030 and uses them to pull the now wetted catheter out of the pouch 1070 via the second compartment 1082.

Before use, the fluid collection bag 1010 may be unfolded to ensure that the collection of liquid within it is not hindered by folds in the fluid collection bag 1010. The handling elements 1031 can be used to handle the catheter 1020 and progressively introduce it into the body until urine flows therethrough and into the fluid collection bag 1010.

Referring to Figures 10-12, after use of the catheter 1020, the user may wish to empty the contents of the fluid collection bag 1010. This can be desirable in order to reduce the size and weight of the used bag 1010 and/or to dispose of the bag 1010. To allow the bag 1010 to be emptied, in this embodiment the outlet 1060 may be removed from the bag 1010 to form an opening 1016 in the peripheral bond between the neck

1050 and notch 1064 as described below.

To form the opening 1016, in this embodiment the user first folds the neck 1050 onto the front panel 1011 of the bag 1010 creating a neck fold-line 1054 parallel to the base 1012 of the peripheral bond and spanning between the end of the left sloped edge

1051 and the end of the right sloped edge 1052 distal the inlet 1053. Advantageously, this helps to ensure fluid in the fluid collection bag 1010 is less likely to pass back into the sleeve 1030 via the inlet 1053 and also ensures the opening 1016 is correctly formed while the outlet 1060 is being removed from the fluid collection bag 1010. In other embodiments, the same effect may be achieved by different means such as deforming, rolling or folding the neck 1050 in different ways.

In this embodiment, the fold in the neck 1050 may be maintained by stowing the used catheter 1020 into the pocket 1017 in the fluid collection bag 1010. The user may do this using the sleeve 1030. Thus, the used and dirty catheter 1020 is retained within the pocket 1017 and is less likely to be accidentally touched during emptying of the fluid collection bag 1010.

In this embodiment, once the neck 1050 is folded, the outlet 1060 is exposed and projects beyond the edge of the bag 1010 which is now defined by the neck foldline 1054. The pull-ring 1062 may then be grasped by the user and pulled in a direction parallel to the neck fold-line 1054 and away from the left lateral edge 1014 to separate the outlet 1060 from the fluid collection bag 1010 forming the opening 1016. Advantageously, the peripheral bond preferentially tears from a point between the right sloped edge 1052 of the neck 1050 and outlet 1060 due to the neck fold-line 1054 which reinforces the peripheral bond around the neck 1050 and reduces tearing forces on the right sloped edge 1052. In addition, the shape of the pull-ring 1062 means that when moved away from the inlet 1053, shearing force is concentrated at the point the outlet 1060 meets the upper edge 1015. This ensures the opening 1016 is created in a controlled manner.

In this embodiment, the notch 1064 provides a second point on the peripheral bond which preferentially forms one end of the opening 1016. Thus, the outlet 1060 may be easily, conveniently, and reliably removed from the fluid collection bag 1010 to form a clean opening 1016 in the peripheral bond. This allows the user to easily empty the contents of the bag 1010 and reduces the risk of spilling the contents of the bag 1010 during emptying.

Referring to Figures 13 to 16, a third embodiment of a packaged catheter assembly 1100 shares many of the features of the first/second embodiments described above and like numerals are used to denote like features.

The assembly 1100 comprises a fluid collection bag 1110, a catheter 1120, a sleeve 1130, a fluid reservoir (not shown, but which may be identical to that in the first embodiment) and a pouch 1170 containing the fluid collection bag 1110, catheter 1120, sleeve 1130 and fluid reservoir. The catheter 1120 has a proximal end 1121 for insertion into the body and a distal end 1122, and the fluid collection bag 1110 is arranged to receive fluid from the distal end 1122 of the catheter 1120.

In this embodiment, the catheter 1120 is a male urinary catheter made from a hydrophilic thermoplastic elastomer (TPE). Obviously those skilled in the art will be able to select suitable alternative examples.

The pouch 1170 is formed from a front wall 1171a and a rear wall 1171b of identical shape and size, two side walls 1171c, and a peripheral seal joining the periphery of the walls to form the pouch 1170 and containing its contents (i.e. the closed catheter assembly and fluid reservoir 1140).

The peripheral seal defines a base 1172a, a left lateral edge 172b, a right lateral edge 1172c and an upper edge 1172d of the pouch 1170. The left lateral edge 1172b and right lateral edge 1172c being defined as the left and right sides of the pouch 1700 when viewing the pouch 1170 with the rear wall 1171b behind the front wall 1171a, the base 1172a at the bottom of the pouch 1170 and the upper edge 1172d at the top of the pouch 1170. The peripheral seal thus defines a pouch 1170 that is generally rectangular and suitably has a width between the lateral edges of between 60-110 mm, preferably 90-110 mm, for example about 100mm, and a height from the base 1172a to the upper edge 1172d of between 100 to 250 mm, preferably 120 to 140 mm, for example about 130 mm. The base 1172a defines the bottom of the pouch 1170 in use, and the upper edge 1172d the top. However, in other embodiments alternative shapes and sizes could be conceived, such as elliptical or circular walls forming correspondingly shaped pouches, or even a tubular pouch or pouch with more than two walls, e.g. a prism or other polygon.

The peripheral seal may be formed from any suitable bonding/sealing methods such as chemical adhesives, chemical bonding, ultrasonic bonding, or mechanical bonding. In alternative embodiments, the pouch 1170 may be formed from a single piece of material. The pouch may then be formed by folding this single piece of material along a pouch fold line to form the walls. In addition, in some embodiments any number of folds may be used to form the pouch 1170. For example, none of the edges may comprise a fold, one edge may comprise a fold (as in the illustrated example), or two or more of the edges may comprise a fold.

In this embodiment, the side walls 1171c are elongate in a direction parallel to the length of the pouch 1170 and extend between the front and rear walls 1171a, 1171b along the left and right lateral edges 1172b, 1172c of the pouch 1170. Along the base 1171a and upper edge 1172d of the pouch 1170, the front and rear walls 1171a, 1171b are sealed to each other directly. As such, in this embodiment, the side walls 1171c allow the front and rear walls 1171a, 1171d to separate to increase the internal volume of the pouch 1170.

In this embodiment, the pouch 1170 is formed from an opaque material and as such provides a discrete package for its contents which can make the user more comfortable in carrying the packaged catheter assembly 1100 in day-to-day life. In addition, the exterior of the pouch 1170 may have a textured or printed appearance, for example a matte appearance, and feel to reduce the impression that it is a medical device.

In this embodiment, the pouch 1170 also comprises an interaction region which forms the majority of the front wall 1171a of the pouch 1170. In this embodiment, the interaction region comprises a break-away region in the form of a rectangular peel- away region 1174. The peel-away region 1174 comprises a base 1174a, left lateral edge 1174b, right lateral edge 1174c and upper edge 1174d that correspond to the base 1172a, left lateral edge 1172b, right lateral edge 1172c and upper edge 1172d of the pouch 1170 respectively. Consequently, the peel-away region 1174 comprises a width between its left lateral edge 1174b and right lateral edge 1174c and a height between its base 1174a and upper edge 1174d. The width of the peel-away region 1174 is between 50-100%, 70-90% or most preferably 80-90% of the width of the pouch 1170, for example 85% of the width of the pouch 1170. The height of the peel-away region 1174 is between 50-100%, 60-90% or most preferably 70-80% of the height of the pouch 1170, for example 75% of the height of the pouch 1170. In this embodiment, the peel-away region 1174 is positioned centrally with respect to the width and height of the pouch 1170. In this embodiment, the comers of the peel-away region 1174 are rounded to provide a smoother and less jagged appearance to the peel-away region 1174. In other embodiments, the comers may not be rounded.

In other embodiments, the break-away region may have a different shape or size as required by the shape/size of the pouch 1170 or the contents of the pouch 1170. It may also not be positioned centrally with respect to the width and/or height of the pouch 1170, for example it may be positioned closer to one edge of the pouch than another.

In this embodiment, the peel-away region 1174 is formed from the same material as the front wall 1171a of the pouch 1170 and is also the same colour to the front wall 1171a, this gives the pouch 1170 a more discreet appearance. In other embodiments, the peel-away region 1174 may be formed of a different material and/or a different colour/shade of colour.

In this embodiment, the front wall 1171a of the pouch 1170 comprises an access aperture 1178a in a position corresponding to the peel-away region 1174. The peel- away region 1174 is attached to the front wall 1171a of the pouch 1170 by a frangible adhesive positioned on the front wall 1171a beneath the base 1174a of the peel-away region 1174. The adhesive 1178b is spread over a rectangular adhesive region 1178b of the front wall 1171a between the access aperture 1178a and base 1172a of the pouch 1170. The adhesive region 1178b has an aspect ratio (length: width) of 1:3 and has a width approximately 50% of the width of the pouch. The adhesive region 1178b is positioned centrally across the width of the pouch 1170 and is completely covered by the peel-away region 1174 when the pouch 1170 is closed. This allows the user to form an opening in the pouch 1170 by peeling the peel-away region 1174 away from the front wall 1171a and breaking the frangible adhesive.

In other embodiments the break-away region may be attached to the front wall 1171a by any suitable bonding/sealing method, for example chemical adhesives, chemical bonding, ultrasonic bonding, or mechanical bonding. In other (tear-away) embodiments, a line of weakness or tear-line in the front wall may define the tear-away region and allow the user to form an opening in the pouch by separating the tear-away region from the front wall. In this embodiment, the peel-away region 1174 is formed from the same piece of material as the front wall 1171a. Consequently, the upper edge 1174d of the peel- away region 1174 is both part of the peel-away region 1174 and part of the front wall 1171a of the pouch 1170 and defines a fold-line about which the peel-away region 1174 may pivot to allow access to the pouch 1170.

In this embodiment, the upper edge 1174d of the peel-away region 1174 is consequently configured not to separate from the front wall 1171a, this prevents the peel-away region 1174 from separating from the pouch 1170 and reduces the number of items that the user must worry about during use of the catheter assembly 1100. In other embodiments, the peel-away region 1174 may be configured to fully separate from the pouch 1170 - for example to allow for easier access to the contents.

In this embodiment, the peel-away region 1174 comprises a front opening tab 1175. The front opening tab 1175 projects from the base 1174a of the peel-away region 1174.

The base 1174a of the peel-away region 1174 comprises straight edges that are slanted towards the centre of the base 1174a. The front opening tab 1175a is positioned at the centre of the base 1174a and spans approximately 50% of the width of the base 1174a. The front opening tab 1175 has a length from the base 1174a to a tip of the front opening tab 1175a that is approximately equal to its width, with a semi-circular end defining the tip.

In this embodiment, the front opening tab 1175 is not adhered to the front wall 1171a of the pouch 1170. The front opening tab 1175 is spaced from the front wall 1171a due to the curvature in the front wall 1171a as it bends to meet the rear wall 1171b at the base 1172a of the pouch 1170. This makes the front opening tab 1175 easier for a user to grasp and open the pouch 1170.

In this embodiment, the base 1172a of the pouch 1170 extends beyond the lateral edges of the front tab 1175 as the front tab 1175 does not extend across the full width of the pouch 1170. This makes it easier to separate the tab 1175 from the pouch 1170. In this embodiment, the front opening tab 1175 comprises an opening marker 1177. The opening marker 1177 comprises a region of the tab 1175 that comprises a logo, marking, a different colour/shade of colour, or different texture/tactile feel than the rest of the tab 1175. In this embodiment, the opening marker 1177 comprises a triangular marker. The marker 1177 is an equilateral triangle positioned centrally on the tab 1177 and pointing towards the centre of the peel-away region 1174. Thus, the marker 1177 directs the user to pull the front opening tab 1175 away from the base 1172a of the pouch 1170 to open the pouch 1170. In other embodiments, a different logo/shape/marker could of course be used to achieve the same effect. In addition, a gripping hole or other tactile element could be used to help the user grasp the tab 1175 more easily.

In this embodiment, the pouch 1170 comprises a first compartment 1181 and a second compartment 1182 separated by an internal wall 1183. The internal wall 1183 comprises a fluid impermeable material that is the same as the material of the front wall 1171a and rear wall 1171b, but, in this embodiment the internal wall 1183 is transparent/translucent to allow the user to see the contents of the first compartment 1181 through the wall 1183. The internal wall 1183 spans the entire width of the pouch 1170 from the left lateral edge 1172b to the right lateral edge 1172c. The internal wall 1183 spans from the base 1172a of the pouch 1170 up approximately 50-90% of the height of the pouch 1170 and most preferably 60% of the height of the pouch 1170. Consequently, an upper (separating) edge 1184 of the internal wall 1183 is revealed when the peel-away region 1174 is at least partially removed from the pouch 1170. The internal wall 1183 is sealed to the pouch 1170 by the peripheral seal which, in this embodiment, seals together the front wall 1171a, internal wall 1183 and rear wall 1171b.

In this embodiment, the internal wall 1183 comprises a cut-away region 1185 cut into the upper edge 1184 of the internal wall 1183. The cut-away region 1185 is centrally located across the width of the pouch 1170 and spans approximately 30% of the width of the peel-away region 1174. The cut-away region 1185 has a semi-circular shape. Of course, in other embodiments the cut-away region 1185 may have any suitable shape, such as rectangular, triangular, ellipsoidal or irregularly shaped. In this embodiment, the upper edge 1184 is sealed to the rear wall 1171b of the pouch 1170 along its entire length except at the cut-away region 1185. This helps to ensure that the contents of each compartment 1181, 1182 does not inadvertently leave each compartment 1181, 1182. The cut-away region 1185 provides access between the first compartment 1181 and second compartment 1182 as the internal wall 1183 is not sealed to either the first wall 1171a or second wall 1171b at the cut-away region 1185.

In this embodiment, the first compartment is defined by the rear wall 1171b and internal wall 1183, and the second compartment is defined by: the internal wall 1183 and the front wall 1171a at locations below the upper edge 1184 of the internal wall 1183; and the rear wall 1171b and front wall 1171a above the upper edge 1184 of the internal wall 1183. Thus, the first and second compartments 1181, 1182 comprise two parallel and planar compartments with access provided between them at the cut-away region 1185 of the internal wall 1183.

In this embodiment, the fluid reservoir is configured to retain a wetting fluid and release wetting fluid to activate the surface of the catheter 1120. In this embodiment, the wetting fluid is water and interacts with the hydrophilic surface of the catheter 1120 to render it lubricious. In other embodiments, other wetting fluids may be used and they may be polar (e.g. water-based) or non-polar (e.g. oil-based) depending on the catheter’s surface properties.

In this embodiment, the fluid reservoir comprises a burstable rectangular sachet positioned within the first compartment 1181 of the pouch 1170 adjacent to the base 1172a of the pouch 1170. The user can release wetting fluid held by the fluid reservoir by compressing the fluid reservoir, for example by pinching it between their fingers. The user can advantageously do this while the fluid reservoir is contained within the pouch 1170 as described in more detail below. To facilitate the user in activating the fluid reservoir, the pouch 1170 comprises a wetting marker 1177 which in this embodiment is the same feature as the opening marker 1177 described above. The wetting marker 1177 comprises a region of the pouch 1170 that is a different colour or texture to the rest of the pouch 1170 to allow the user to easily identify the position of the fluid reservoir and where to press to activate it and release wetting fluid into the pouch 1170. In this embodiment, the wetting marker 1177 is disposed on the peel-away region 1174. In other embodiments, the fluid reservoir may be configured to release wetting fluid through a different means, for example by twisting or bursting the fluid reservoir in a different way.

In this embodiment, the fluid collection bag 1110 comprises a front panel 1111a, a rear panel 111 lb of identical shape and size and a base panel 111 Id that spans between the front panel 1111a and rear panel 1111b. A peripheral bond joins the peripheries of the panels to form the bag 1110. The peripheral bond defines a base 1112, a right lateral edge 1113, a left lateral edge 1114 and an upper edge 1115. The right lateral edge 1113 and left lateral edge 1114 being defined as the right and left sides of the bag 1110 when viewing the bag 1110 with the rear panel 1111b behind the front panel 1111, the base 1112 at the bottom of the bag 1110 and the upper edge 1115 at the top of the bag 1110. The peripheral bond thus defines a bag 1110 that is generally rectangular and suitably has a width between the lateral edges of between 10 and 20 cm, and most preferably between 12 and 15 cm, and a height from the base 1112 to the upper edge 1115 of between 25 and 40 cm, 30 and 35 cm, or most preferably 33 and 35 cm. The bag is thus configured to hold at least 700 ml of fluid released from the user through the catheter safely. The base 1112 defines the bottom of the bag 1110 in use, and the upper edge 1115 the top. However, in other embodiments alternative shapes and sizes could be conceived, such as elliptical or circular panels forming correspondingly shaped bags, or even a tubular bag or bag with more than two panels, e.g. a prism or other polygon.

Notably, in this embodiment, the fluid collection bag 1110 comprises a base panel 111 Id that spans between the front panel 1111a and rear panel 1111b along the base 1112 of the peripheral bond. The base panel 111 Id is lens shaped in that it has two curved edges bounding a convex region. The curved edges are joined to the base edges of the front and rear panels 1111a, 1111b respectively and the vertices where the curved edges meet are at the left and right lateral edges 1113, 1114 of the fluid collection bag 1110. The base panel 111 Id allows the front panel 1111a and rear panel 111 lb to separate along the base 1112.

Consequently, the base panel 111 Id allows the fluid collection bag 1110 to have a greater internal volume and also to be free-standing when partially filled with fluid as described below. The base 1112 is formed by two flanges 1112A, 1112B ; the rear panel joined to the base panel by the peripheral bond forms a first flange 1112A and the front panel joined to the base panel by the peripheral bond forms the second flange 1112B. The two flanges 1112A, 1112B extend from the two curved edges where the base panel 111 Id meets the rear panel 1111b and the front panel 1111a respectively.

In this embodiment, the front, rear and base panels 1111a, 1111b, l l l ld comprise a flexible plastics material, for example polypropylene (PP), polyethylene terephthalate (PET), low density polyethylene (LDPE), metalized polyester (MET PET) orientated polypropylene (OPP), polyvinylpyrrolidone (PVP), or polyvinyl chloride (PVC).

In this embodiment, the upper edge 1115 of the bag 1110 is tapered towards a neck 1150 which facilitates the fluid connection between the fluid collection bag 1110 and the catheter 1120. The neck 1150 is positioned adjacent to the right lateral edge 1113 of the fluid collection bag 1110 and spans the right hand third of the upper edge 1115. The neck 1150 has an aspect ratio (length: width) of 2: 1 at its base and is tapered such that its width is reduced by approximately 20-50% at its tip, which is flat with rounded comers.

In this embodiment, the neck 1150 comprises an inlet 1153 positioned centrally on the neck 1150 and in the front panel 1111a of the bag 1110. The inlet 1153 is configured to receive the catheter 1120 and comprises an aperture through which the catheter 1120 projects and in which the catheter 1120 is retained.

In this embodiment, the fluid collection bag 1110 is a closed bag that is not intended to release fluid contained within it. However, in other embodiments, the fluid collection bag 1110 may comprise an outlet to allow fluid to be released from the bag 1110.

In this embodiment, the fluid collection bag 1110 also comprises a retaining element in the form of a strap 1117. The strap 1117 is configured to retain the fluid collection bag 1110 in a stowed (rolled) configuration before use. The strap 1117 comprises a strip of material configured to extend all the way around the rolled bag 1110 and seal to itself, for example through a chemical adhesive, hook-and-hook, or hook-and-loop fasteners. In this embodiment, hook-and-hook type fasteners are used to allow re-sealable adhesion to a variety of surfaces/objects as described further below. Alternatively, a re-sealable adhesive such as an epoxy resin or alternatively a silicone- based adhesive may be used. In addition, one end of the strap 1117 is permanently adhered to the front panel 111 la of the fluid collection bag 1110 for example through a weld, to ensure the strap 1117 does not become fully detached from the bag 1110 and is easier to use.

In this embodiment, the strap 1117 is also configured to releasably attach the rolled fluid collection bag 1110 to the underside of the peel-away region 1174. Consequently, when the pouch 1170 is opened, the fluid collection bag 1110 is pulled through the access aperture 1178a as it remains on the underside of the peel-away region 1174 until the user removes it from the pouch 1170 as described below.

In this embodiment, the strap 1117 is also configured to retain the catheter 1120 in a stowed (folded) configuration after use. The catheter 1120 may be coiled and then sealed against the bag 1110 using the strap 1117. The upper region of the bag 1110 adjacent to the upper edge 1115 may be folded (with the front panel 111 la on the inside of the fold) and the strap 1117 attached to (the rear panel 1111b of) the bag 1110 to retain the bag 1110 in the folded configuration with the catheter 1020 stowed against it. Thus, the bag 1110 and catheter 1120 are more convenient to carry and dispose of after use.

In this embodiment, the strap 1117 comprises a release mechanism in the form of a pull-tab 1118 which is a short section of the strap 1117 that is configured to be pulled by the user to release the strap 1117. In this embodiment, the pull-tab 1118 is the end of the strap 1117 distal from the end permanently attached to the fluid collection bag 1110.

In this embodiment, the pull-tab 1118 comprises a release marker in the form of a pull-marker 1119. The pull-marker 1119 is a region of the pull-tab 1178 that comprises a logo, marking, a different colour/shade of colour, or different texture/tactile feel than the rest of the tab 1178. In this embodiment, the pull-marker 1119 comprises a triangular marker. The marker 1119 is an equilateral triangle positioned centrally on the tab 1119 and pointing towards the opposite end of the strap 1117. Thus, the marker 1119 directs the user to pull the tab 1118 to release the strap 1117. In other embodiments, a different logo/shape/marker could of course be used to achieve the same effect. Of course, the marker 1119 may be recognisable both visually and by touch. In addition, a gripping hole or other tactile element could be used to help the user grasp the tab 1118 more easily.

In this embodiment, the distal end 1122 of the catheter 1120 comprises a funnel 1123. The funnel 1123 is positioned within the fluid collection bag 1110 and comprises a relatively rigid material, such as HDPE, compared to the fluid collection bag 1110. The funnel 1123 is sized such that it cannot pass through the inlet 1153 and as such, is configured to prevent removal of the catheter 1120 from the fluid collection bag 1110.

In this embodiment, the fluid collection bag 1110 is provided in a stowed folded configuration and in a different compartment as the fluid reservoir, consequently, the fluid collection bag 1110 is provided in the second compartment 1182 attached to the peel-away region 1174 as mentioned above. The inlet 1153 is positioned closer to the cut-away region 1185 and upper edge 1184 of the internal wall 1183 than the rest of the stowed fluid collection bag 1110 and the catheter 1120 extends from the inlet 1153 between the upper edge 1184 of the internal wall 1183 and upper edge 1172d of the pouch 1170 into the first compartment 1181.

The position and configuration of the catheter 1120 in the first compartment 1181 is not particularly limited so long as it is not curved to the extent that damage to the catheter is likely, for example from kinking. In this embodiment, the catheter 1120 is arranged within the first compartment 1181 in a curved/coiled configuration, this helps ensure that the catheter 1120 is not excessively curved and minimises risk of damage.

In this embodiment, the sleeve 1130 comprises two handling elements 1131. Each handling element 1131 comprises a tubular sheet material through which the catheter 1120 extends and which allows the handling element 1131 to be moved along the length of the catheter 1120. Each handling element 1131 is approximately 2-8 cm in length, preferably 3-7 cm, for example 5 cm in length. Consequently, each handling element 1131 and both handling elements 1131 together span a minority of the length of the catheter 1120. This leaves the majority of the catheter 1120 uncovered and as such easily wetted by wetting fluid released from the fluid reservoir as described below.

In this embodiment, the sleeve 1130 comprises a line of weakness 1132 that may be broken to form the two handling elements 1132. This simplifies manufacture of the catheter assembly and can allow the handling elements 1131 to more securely remain in a given position prior to use. In this embodiment, the line of weakness 1132 comprises a line of perforations around the circumference of the sleeve 1130. In other embodiments, the handling elements 1132 may be independent but sealed together by a temporary seal present between them, for example a tack weld. In other embodiments, each handling element 1131 may be independent of the other and not adhered or sealed to the other.

While in this embodiment the sleeve 1130 comprises two handling elements 1131, in other embodiments, the sleeve 1130 may comprise a single handling element 1131 or more than two handling elements 1131 as required.

In this embodiment, one handling elements 1131 is located in a position corresponding to the cut-away region 1185 such that its position is restricted and it is easily accessible to the user when opening the pouch 1170. In this position, the handline element 1131 also helps to prevent liquid from passing through the cut-away region 1185 and into the second compartment 1182. As described above, the fluid reservoir is arranged in the first compartment 1181 and the catheter 1120 extends from the fluid collection bag 1110 into the first compartment 1181.

Prior to use, the pouch 1170 is provided sealed closed with the contents arranged within it as mentioned above. To ensure the catheter 1120 is wetted prior to use, the user must activate the fluid reservoir by locating it within the pouch 1170 and squeezing it to rupture the fluid reservoir and release wetting fluid into the first compartment 1181. This can be done with the aid of the wetting marker 1177 on the outside of the pouch 1170.

Advantageously, once wetting fluid is released into the first compartment 1181 it is prevented from reaching the fluid collection bag 1110 and sleeve 1130 by the internal wall 1183. This ensures that the wetting fluid is most efficiently used to wet Ill the catheter 1120, the majority of which is in the first compartment including the proximal end 1121 of the catheter. In addition, it ensures that the fluid collection bag 1110 and sleeve 1130 remain dry and easier to handle.

Once the catheter 1120 has been wetted, the contents of the pouch 1170 can be accessed by opening the pouch 1170. The pouch 1170 is opened by separating the opening tab 1175 from the pouch 1170 to break the adhesive at the adhesive region 1178b. As the tab 1175 and pouch 1170 are separated, the peel-away region 1174 peels away from the front wall 1171a of the pouch 1170 revealing the contents of the second compartment 1182.

Once the pouch 1170 has been opened, which in some embodiments may involve completely removing the break-away region from the pouch 1170, the fluid collection bag 1110, catheter 1120 and sleeve 1130 may be removed from the pouch 1170. Preferably, the user grasps the dry folded stowed fluid collection bag 1110, for example using the pull-tab 1118, and/or one or both dry handling elements 1131 of the sleeve 1130 and uses them to pull the now wetted catheter out of the pouch 1170 via the second compartment 1182.

Before use, the fluid collection bag 1110 must be unrolled to ensure that the collection of liquid is possible. This can be done by pulling the pull-tab 1118 in the direction of the pull-marker 1119 with respect to the rest of the bag 1110 to release the strap 1117 and unroll the bag 1110. The handling elements 1131 can be used to handle the catheter 1120 and progressively introduce it into the body until urine flows therethrough and into the fluid collection bag 1110.

In this embodiment, the base panel 111 Id of the bag 1110 is initially provided in a stowed configuration in which it is folded up between the front and rear panels 1111a, 1111b. As liquid 1101 enters the bag 1110, the front and rear panels 1111a, 1111b may be separated and the base panel 11 Id unfolded such that it is flat and substantially perpendicular to the front and rear panels 1111a, 1111b. Liquid 1101 inside the bag 1110 collects at the base panel 111 Id and consequently, the bag 1110 is able to stand up while it is filled. This provides additional convenience to the user as they need not hold or hand the bag during use. Once the user has emptied their bladder, the catheter 1120 may be removed from the body, for example using the sleeve 1130/handling elements 1131. The catheter 1120 may then be folded/coiled and stowed against the fluid collection bag 1110 using the strap 1117. As mentioned above, the fluid collection bag 1110 may be folded close to the upper edge 1115 and the folded/coiled catheter 1120 collected adjacent to the neck 1150. The strap 1117 is then used to secure the fluid collection bag 1110 and catheter 1120 in this position by attaching it to the fluid collection bag 1110, for example on the rear panel 1111b. The fluid collection bag 1110 and catheter 1120 are then in a conveniently arranged for disposal or storage until disposal.

While the embodiments disclosed above are described as a closed catheter assembly in that fluid is collected in a fluid collection bag, other embodiments may not comprise a fluid collection bag and may be open catheter assemblies in that fluid is not collected during use. Likewise, whilst the embodiments above describe each include two or more the inventive aspects, it will be understood that they are not intrinsically linked, for example the baffled fluid collection bag could be arranged in a pouch of entirely different construction; the pouch could contain a fluid collection bag of conventional construction, without the baffles, and the two-compartment concept need not be combined with the arrangement of the fluid collection bag at the opening of the pouch.

Of course, the sizes and shapes set out above as well as choice of materials and so forth are exemplary.

The one or more embodiments are described above by way of example only. Many variations are possible without departing from the scope of protection afforded by the appended claims.

Claims

CLAIMS A packaged catheter assembly comprising a catheter, a fluid reservoir comprising wetting fluid, and a pouch, wherein: the pouch is divided into first and second compartments; the fluid reservoir and at least a portion of the catheter are arranged in the first compartment; and a fluid collection bag is connected to the catheter and is arranged in the second compartment; and the fluid reservoir is configured to release the wetting fluid into the first compartment to wet the catheter. A packaged catheter assembly according to claim 1, wherein the pouch comprises an interaction region operable by a user to form an opening in the pouch allowing access to at least the second compartment. A packaged catheter assembly according to claim 2, wherein the opening allows access to the first compartment and optionally wherein access to the first compartment is via the second compartment. A packaged catheter assembly according to any preceding claim, wherein the pouch comprises a front wall and a rear wall, a peripheral seal between the two walls, and an internal join, joining the walls to divide the pouch into the first and second compartments. A packaged catheter assembly according to claim 4, wherein the internal join is arranged to inhibit wetting fluid from the fluid reservoir wetting the second compartment and the fluid collection bag arranged therein. A packaged catheter assembly according to claim 4 or 5, wherein the internal join defines a channel having a diameter which is substantially equal to the diameter of the catheter at the channel, and further wherein the catheter is arranged such that before withdrawal of the catheter from the pouch, a portion of the catheter is positioned within the channel. A packaged catheter assembly according to claim 6, wherein the interaction region is arranged at one edge of the pouch and the channel is arranged adjacent to the interaction region; and wherein the internal join extends from the peripheral seal to the channel. A packaged catheter assembly according to any of claims 1 to 3 wherein the pouch comprises a front wall and a rear wall, a peripheral seal between the two walls, and an internal wall defining the first and second compartments. A packaged catheter assembly according to claim 8 wherein the first compartment comprises the rear wall and internal wall and the second compartment comprises the front wall and internal wall. A packaged catheter assembly according to claim 8 or 9 wherein the internal wall is attached to the pouch by the peripheral seal. A packaged catheter assembly according to any of claims 8 to 10 wherein the internal wall spans the entire width of the pouch. A packaged catheter assembly according to any of claims 8 to 11 wherein the internal wall comprises a separating edge and access between the first and second compartments is provided at or adjacent to the separating edge. A packaged catheter assembly according to claim 12 wherein the separating edge comprises a cut-away region and the catheter is arranged such that before withdrawal of the catheter from the pouch, a portion of the catheter is positioned within the cut-away region. A packaged catheter assembly according to claim 12 or 13 wherein the separating edge is sealed along part of its length to the front or rear wall. A packaged catheter assembly according to any preceding claim, wherein the pouch is configured such that after release of the wetting fluid into the first compartment, the wetting fluid is retained in the first compartment and the second compartment remains free from wetting fluid. A packaged catheter assembly according to claim 2, wherein the interaction region is configured such that before withdrawal of the catheter from the pouch, the opening comprises a sterile seal. A packaged catheter assembly according to claim 16, wherein the sterile seal is broken by tearing off a removable tear strip. A packaged catheter assembly according to claim 16, wherein the sterile seal is broken by peeling a peel-away region from the pouch. A packaged catheter assembly according to any preceding claim, wherein the fluid collection bag comprises a front panel and a rear panel, and a peripheral bond between the two panels defining an internal cavity; wherein the cavity is provided with a plurality of internal baffles. A packaged catheter according to claim 19 wherein, each baffle extends inwardly from the peripheral bond of the fluid collection bag. A packaged catheter assembly according to claim 20, wherein each baffle is provided by a join joining the front panel of the fluid collection bag to the rear panel of the fluid collection bag. A packaged catheter assembly according to any of claims 19 to 21, wherein the plurality of internal baffles are arranged as diametrically opposed pairs of baffles, wherein each baffle extends inwardly toward the opposing baffle in the pair to form a channel therebetween. A packaged catheter assembly according to any preceding claim, wherein the fluid collection bag is provided in a stowed configuration. A method of manufacturing a packaged catheter assembly comprising the steps of providing a catheter, a fluid reservoir comprising wetting fluid, a fluid collection bag and a pouch divided into first and second compartments; arranging the fluid reservoir and at least a portion of the catheter in the first compartment; connecting the fluid collection bag to the catheter; and arranging the fluid connection bag in the second compartment; wherein the pouch is configured to provide an opening allowing access to at least the second compartment, and through which the catheter may be withdrawn. The method according to claim 24 wherein the pouch comprises front and rear walls and the method further comprises providing an internal wall to divide the pouch into the first and second compartments and sealing a separating edge of the internal wall to the front or rear wall of the pouch. A method of unpackaging a packaged catheter assembly, the packaged catheter assembly comprising a catheter, a fluid reservoir comprising wetting fluid, and a pouch, wherein: the pouch is divided into first and second compartments; the fluid reservoir and at least a portion of the catheter are arranged in the first compartment; and a fluid collection bag is connected to the catheter and arranged in the second compartment; the method comprising releasing the wetting fluid into the first compartment so as to wet the catheter arranged therein; forming an opening in the pouch allowing access to at least the second compartment and removing the catheter from the second compartment. The method of claim 26 comprising removing the fluid collection bag from the pouch before removing the catheter. The method of claim 26 or 27 comprising rupturing/bursting/opening the fluid reservoir within the pouch. The method of claim 28 comprising locating the fluid reservoir within the pouch via a window in the pouch and/or a wetting marker disposed on the pouch.

30. The method of any of claims 24 to 29, wherein the packaged catheter assembly is the packaged catheter assembly of any of claims 1 to 23.