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WO2020052616A1 - 用于生殖系统的设备 - Google Patents

用于生殖系统的设备 Download PDF

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Publication number
WO2020052616A1
WO2020052616A1 PCT/CN2019/105521 CN2019105521W WO2020052616A1 WO 2020052616 A1 WO2020052616 A1 WO 2020052616A1 CN 2019105521 W CN2019105521 W CN 2019105521W WO 2020052616 A1 WO2020052616 A1 WO 2020052616A1
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WO
WIPO (PCT)
Prior art keywords
fluid
pressure
reproductive system
cavity
human body
Prior art date
Application number
PCT/CN2019/105521
Other languages
English (en)
French (fr)
Inventor
李辉
Original Assignee
李辉
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 李辉 filed Critical 李辉
Publication of WO2020052616A1 publication Critical patent/WO2020052616A1/zh

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H19/00—Massage for the genitals; Devices for improving sexual intercourse
    • A61H19/40—Devices insertable in the genitals
    • A61H19/44—Having substantially cylindrical shape, e.g. dildos
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H19/00—Massage for the genitals; Devices for improving sexual intercourse
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H21/00—Massage devices for cavities of the body, e.g. nose, ears and anus ; Vibration or percussion related aspects A61H23/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H23/00—Percussion or vibration massage, e.g. using supersonic vibration; Suction-vibration massage; Massage with moving diaphragms
    • A61H23/02—Percussion or vibration massage, e.g. using supersonic vibration; Suction-vibration massage; Massage with moving diaphragms with electric or magnetic drive
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H9/00—Pneumatic or hydraulic massage
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H9/00—Pneumatic or hydraulic massage
    • A61H9/005—Pneumatic massage
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H9/00—Pneumatic or hydraulic massage
    • A61H9/005—Pneumatic massage
    • A61H9/0078—Pneumatic massage with intermittent or alternately inflated bladders or cuffs
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M31/00—Devices for introducing or retaining media, e.g. remedies, in cavities of the body
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H2201/00—Characteristics of apparatus not provided for in the preceding codes
    • A61H2201/10—Characteristics of apparatus not provided for in the preceding codes with further special therapeutic means, e.g. electrotherapy, magneto therapy or radiation therapy, chromo therapy, infrared or ultraviolet therapy
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H2201/00—Characteristics of apparatus not provided for in the preceding codes
    • A61H2201/10—Characteristics of apparatus not provided for in the preceding codes with further special therapeutic means, e.g. electrotherapy, magneto therapy or radiation therapy, chromo therapy, infrared or ultraviolet therapy
    • A61H2201/105—Characteristics of apparatus not provided for in the preceding codes with further special therapeutic means, e.g. electrotherapy, magneto therapy or radiation therapy, chromo therapy, infrared or ultraviolet therapy with means for delivering media, e.g. drugs or cosmetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2210/00—Anatomical parts of the body
    • A61M2210/10—Trunk
    • A61M2210/1042—Alimentary tract
    • A61M2210/1067—Anus
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2210/00—Anatomical parts of the body
    • A61M2210/14—Female reproductive, genital organs

Definitions

  • the invention relates to a device for the reproductive system, which can be used for the treatment of female infertility, male semen liquefaction, prostatitis, female ovaries, uterus, fallopian tubes, vaginal health care, eugenics and eugenics.
  • the treatment technology in this aspect is mainly to use a hard metal wire for dredging, or to cut off the clogged part by surgery, and then bond the cut off residual part. Because these methods directly damage the tissue of the blocked fallopian tube, they are more likely to cause blockage again after dredging.
  • the purpose of the present invention is to provide a novel device and treatment method for solving the problems of female infertility, male semen liquefaction, male infertility, prostatitis, and ovarian, uterine, vaginal and fallopian tube health care.
  • a device for a female reproductive system which is composed of at least a control part, a fluid excitation device (a fluid excitation device refers to a device for applying pressure to a fluid, and changing a fluid pressure), and human contact.
  • the human body contact end refers to the parts that come into contact with the human body.
  • the human body contact end can be in contact with the human body to form a sealed contact surface.
  • the fluid excitation device is connected to the human body contact end (directly or indirectly. When directly connected, the human body The contact end is directly arranged on the fluid excitation device, and the indirect connection can be connected through a pipe.)
  • the control parts and the fluid excitation device are connected to control the operation of the fluid excitation device.
  • the fluid excitation device acts on the fluid to generate the fluid.
  • Pressure fluid pressure (directly or indirectly, positive pressure, negative pressure) acts on the human body.
  • the contact position may be the female genitals, vagina, uterus, cervix, fallopian tube, uterus and fallopian tube intersection and the vicinity.
  • the simplest form of control component is a power plug, and the more complex is an integrated circuit.
  • the fluid can be a gas or a liquid.
  • the above-mentioned equipment adopts an electric-driven fluid excitation device.
  • the fluid may be a combination of a gas and a liquid.
  • Drug-containing liquids are placed in the uterus, while the device itself can use gas or liquid.
  • gas can be used directly in the womb without fluid.
  • the fluid is in direct contact with the human body without spacers.
  • the pressure of the fluid changes with time, and the pressure rise and fall cycles are performed.
  • the pressure of the fluid generated by the fluid excitation device changes periodically.
  • High-frequency pressure and pressure change can form a vibration massage effect on the female reproductive system.
  • the contact end of the human body can enter the uterus and be in contact with the uterus and fallopian tubes.
  • the contact end of the human body is provided with an expandable fluid cavity. After the fluid is filled in the cavity, the cavity is expanded, and the outside of the cavity is fitted and sealed with the human body.
  • a safety valve, a maximum pressure adjusting part, and a pressure measuring part may be provided in a fluid pipeline communicating with the human body.
  • the device is provided with means for regulating the pressure of the fluid.
  • the device has means for manually adjusting the magnitude of the fluid pressure to determine the maximum pressure that the user can withstand.
  • the device is provided with a frequency, fluid displacement adjustment device.
  • the fluid excitation device may be: installing an oscillator (eccentric motor, etc.) on the elastic wall of the elastic fluid cavity. You can also install other common fluid pressure boosting devices or modified devices, such as various water pumps and air pumps.
  • the range of pressure change can be negative to positive, 0 to positive, 0 to negative, or any other data range.
  • a fixing device can be added to the human contact end to fix the human contact end on the human body.
  • the shape depends on the female vulva shape and is made of soft rubber material. The user can sit on it and press the contact end made of elastic material with his own gravity to seal the contact end.
  • a ring-shaped vacuum suction band is set around the vaginal opening and sealed by suction vacuum.
  • the inner layer is a rigid hollow tube, and the outer layer of the hollow tube is installed with a fluid elastic bladder.
  • the fluid elastic bladder is filled with air or liquid to expand and elastic.
  • the periphery of the sac and the vagina are tightly pressed tightly, thereby sealing.
  • the above-mentioned elastic capsules may be several annular balloons arranged along the vaginal axis.
  • the above technical schemes and features can be applied to equipment for treating male semen liquefaction and prostatitis.
  • the device's human contact end is placed inside the rectum or outside the anus.
  • the contact end of the human body is an open, sealable container, and the male reproductive organ (partial or full) can be placed in the container. Organs such as the scrotum and testes can enter and exit the container through the opening.
  • the opening has sealing parts, which can seal the opening and the contact surface of the human body.
  • the invention provides a method for treating female infertility.
  • the fluid is used to apply pressure to the female reproductive system cavity over time.
  • the pressure of the fluid changes periodically.
  • the invention provides a method for female health care, which uses fluid to exert pressure on the cavity of the female reproductive system over time, thereby exerting force on female reproductive organs such as the fallopian tube, ovary, and uterus.
  • the pressure of the fluid changes periodically.
  • the female reproductive system cavity mentioned above includes: vagina, cervix, uterus, fallopian tubes, ovaries.
  • the invention provides a female health-care device, which is composed of at least one resistance component, an expandable fluid cavity, and a fluid filling and discharging device.
  • the fluid filling and discharging device is connected to the expandable fluid cavity and can fill fluid into the expandable A fluid cavity. After the fluid is filled into the cavity, the cavity expands. The periphery of the cavity fits the human body.
  • the resistance part and the expandable fluid cavity exist in such a part. They exist at the same time in the axial section of the vagina (that is, That is, the expandable fluid cavity and the resistance member are placed side by side in the vagina or the fluid cavity surrounds the resistance member, rather than being placed in the vagina in series along the vaginal axis). If an elastic container has a small internal volume without being filled with fluid, and the internal volume becomes larger after being filled with fluid, then it is expandable.
  • At least one of the cavity mentioned is in communication with the damping adjustment device (including the case where the damping adjustment device is located in the cavity, which still belongs to the communication); the other is connected with the fluid filling and discharging device (such as a hand pressure airbag) .
  • the pressure sensor is located between the damping adjustment device and the stressed portion of the resistance member.
  • the present invention provides a female health care device, which is composed of at least a human contact end, a resistance member, a fluid excitation member, a control member, and the like.
  • the human contact end is connected through the resistance member and the fluid excitation member (the resistance member is also located inside the human contact end.
  • the control part is connected to the fluid excitation part.
  • the resistance part contains a damping valve. The fluid enters and exits the fluid excitation part and the human contact end through the damping valve.
  • the control part can control the operation of the fluid excitation part.
  • the fluid excitation part can pass the fluid through the damping.
  • the valve is pressed back to the human contact end.
  • the resistance generated when the fluid is squeezed out of the human contact end through the damping valve can provide resistance to the muscle contraction in the female pelvic cavity; after the fluid enters the human contact end, the muscle in the female pelvic cavity contracts and squeezes the human contact end, thereby passing the fluid through The damping valve pushes out the contact end of the human body.
  • the resistance of the damping valve is adjustable.
  • the damping valve is a one-way valve.
  • the damping is small, and the damping is large.
  • the fluid excitation component is driven by electricity.
  • the invention also provides a device to be placed in the rectum, which is composed of at least one vibrating member, an expandable fluid cavity, and a fluid filling and discharging device.
  • the fluid filling and discharging device is connected to the expandable fluid cavity, and the fluid An expandable fluid cavity is filled. After the fluid is filled into the cavity, the cavity expands and the periphery of the cavity fits the human body.
  • the vibrating member is connected to the expandable fluid cavity, and the vibrating member and the expandable fluid cavity exist in such a part that they coexist in the rectal axial section at the same time.
  • the vibration member is installed in a rigid tube, and the expandable fluid cavity is installed outside the rigid tube and communicates with the fluid filling and discharging device.
  • all the above solutions can be provided with a mobile phone APP supporting a mobile phone to control the operation of related equipment and display operating parameters.
  • relevant operating parameters can also be displayed via a special display device.
  • the present invention repeatedly bends and resets the fallopian tube adhesion through repeated changes in pressure, causing fatigue damage to different tissues (adhesive human tissue, obstructions, and fallopian tubes) at the microscopic level.
  • the size of the breakage is small, and gradually break away. It can be repaired gradually by using it for a certain period of time every day and accumulated over multiple days. It is slowly broken and repaired slowly, and the damaged part is gradually repaired, so it is not easy to relapse and adhesion.
  • the metal wire directly breaks the adhesion tissue is a one-time forced breakage of the adhesion tissue, and the wound is relatively large. When such a large wound is repaired by itself, the two fractures are easily adhered again.
  • the repeated changes in pressure also cause the wall of the fallopian tube to bend repeatedly.
  • the elasticity of the tube wall will be enhanced, and the entire fallopian tube will expand under pressure, which is more conducive to the movement of eggs and fertilized eggs.
  • the repeated application of pressure to the female genital cavity by fluid can exercise the female genital cavity, uterus, fallopian tubes, and ovaries, which is conducive to improving and strengthening the functions of these organs and the quality of the eggs produced, thereby achieving The purpose of eugenics.
  • FIG. 1 is a three-dimensional perspective view of an assembly according to Embodiment 1 of the present invention.
  • FIG. 2 is a three-dimensional perspective view of the assembly of Embodiment 1 of the present invention.
  • FIG. 3 is a cross-sectional view of the assembly 18 in FIG. 2.
  • FIG. 4 is a cross-sectional view of the component 18 in FIG. 2 after it is expanded.
  • FIG. 5 is a three-dimensional cross-sectional view of a human body contacting terminal selected in Embodiment 1 of the present invention.
  • FIG. 6 is a three-dimensional cross-sectional view of another human contacting end selected in Embodiment 1 of the present invention.
  • FIG. 7 is a three-dimensional cross-sectional view of another human contacting end selected in Embodiment 1 of the present invention.
  • FIG. 8 is a front perspective view of a complete machine assembly according to Embodiment 2 of the present invention.
  • FIG. 9 is a three-dimensional perspective view of a complete machine assembly according to Embodiment 2 of the present invention.
  • FIG. 10 is a cross-sectional view of the assembly 38 in FIG. 8.
  • FIG. 11 is a three-dimensional perspective view of the component 45 in FIG. 10.
  • FIG. 12 is a three-dimensional perspective view of the component 44 in FIG. 10.
  • FIG. 13 is a three-dimensional perspective view of the component 38 in FIG. 8 after being expanded.
  • FIG. 14 is a front view of a complete machine assembly according to Embodiment 3 of the present invention.
  • FIG. 15 is a three-dimensional perspective cross-sectional view of a complete machine assembly according to Embodiment 3 of the present invention.
  • FIG. 16 is a cross-sectional view of the assembly 59 in FIG. 14.
  • FIG. 17 is a three-dimensional perspective view of a complete machine assembly according to Embodiment 4 of the present invention.
  • Figure 10 39, airbag base; 40, fixed ring; 41, end cap; 42, airbag outer cover; 43, inner sleeve; 44, inner tube; 45, one-way valve base; 46, one-way valve; 47 , Fixed ring; 48, fixed ring; 49, end cover; 50, resistance adjustment cover; 51, sleeve; 52, catheter; 53, pressure gauge; 54, air bag;
  • Example 1 is an embodiment of the device for treating female infertility according to the present invention.
  • the stepping motor assembly 9, the motor 10, and the pendulum block 14 are all installed on the carriage 13; the motor 10 drives the crank 11 to rotate. Hole, so the crank 11 can drive the guide rod 7 to swing.
  • the guide rod 7 passes through the slider 8, and the slider 8 and the right end of the piston rod of the piston assembly 6 form a rotating pair, so when the guide rod 7 swings left and right, the piston assembly 6 can be moved left and right.
  • the carriage 13 can slide on the frame 17.
  • a gear is mounted on the stepper motor assembly 9.
  • the gear meshes with the rack on the frame 17, so the stepper motor assembly 9 can control the carriage 13 on the frame 17. slide.
  • the swing amplitude of the guide rod 7 can be changed. Therefore, the single exhaust volume of the piston cylinder can be changed, thereby changing the air flow rate that is finally pressed into the human body.
  • the gas in the cylinder 4 enters the human body contact end assembly 18 through the conduit 1 and finally enters the human body.
  • the final maximum fluid pressure inside the human body can be set to ensure safety.
  • the pressure gauge 16 and the air pump 172 are connected to the piston cylinder 4 through a conduit.
  • the pressure gauge 16 shows the pressure in the piston cylinder, that is, the pressure actually applied to the human body.
  • the rotation of the crank 11 can be driven by the electric motor 10 or by shaking the hand wheel 12.
  • the hand wheel 12 can be slowly moved by the manual operation of the hand wheel 12, so it can be used for fine adjustment and testing.
  • the inflation and deflation function of the airbag 19 can also be performed by the air pump 172, as long as the corresponding conduits, valves, and control procedures are modified.
  • the airbag cover 25 is made of a soft and elastic material (such as latex) and can be expanded and deformed.
  • the airbag 19 (see FIG. 3) is connected to the hole of the airbag base 22 through the catheter 20 so as to be connected with the cavity between the inner tube 24 and the airbag cover 25.
  • the airbag cover 25 is fixed and sealed to one end of the inner tube 24 by a fixing ring 26; the other end is fixed and sealed to the outside of the airbag base 22 by a fixing ring 23.
  • the airbag base 22 is fixed to the periphery of the inner tube 24.
  • the end cap 21 and the inner tube 24 are fixed.
  • the end cap 21 is connected to the catheter 1 in FIG. 2.
  • the air pump 172 pressurize the gas into the patient's body to apply pre-pressure, and ask the patient how they feel.
  • the pressure of the pressure gauge 16 is the maximum that the patient can use pressure.
  • the determination of the maximum pressure that the patient can withstand can also be accomplished by manually shaking the hand wheel 12.
  • the reciprocating pushing of the piston assembly 6 can also be completed by a push-pull electromagnet, an eccentric motor, a crank slider structure, or other common mechanical structures capable of achieving linear motion (for details, refer to books on mechanical principles).
  • the frequency of pressure changes in the genital cavity can be changed.
  • Figures 5, 6, and 7 are the other forms of the human contact end, respectively.
  • the catheter on the top right side in FIG. 6 can be connected with a vacuum-extracting component, thereby forming a negative pressure and adsorbing to the human body.
  • the second embodiment shown in FIG. 8 is a case where the present invention is applied to a female pelvic floor exerciser.
  • the resistance member 38 is placed in the user's vagina.
  • the pressure gauge 27 and the airbag 28 are connected to the cavity in the resistance member 38 through the catheter 29.
  • the airbag cover 42 is made of a soft material (such as latex), is elastic, and can be expanded and deformed.
  • the inner sleeve is also made of a soft material (such as silicone) and can be compressed inward.
  • the airbag 54 ie, the airbag 28 in FIG. 8) is repeatedly squeezed by hand to press gas into the sealed cavity between the airbag outer cover 42 and the inner sleeve 43.
  • the piston assembly 33 is locked and fixed by the control member, so when the airbag 54 is inflated, the inner sleeve 43 cannot be compressed inward.
  • the inflation can be stopped, and the piston assembly 33 is unlocked.
  • FIG. 13 shows a state after the airbag cover 42 is inflated.
  • the user contracts the muscles around the vagina, compresses the airbag jacket 42 inward, and then compresses the inner sleeve 43.
  • the liquid in the inner sleeve 43 enters the inner tube 44 through the damping hole in the middle of the inner tube 44, and then passes through the catheter 30 and enters the piston cylinder 34.
  • Push the piston assembly 33 to move to the right there is a unidirectional ratchet in the gear 37, so when the piston assembly 33 moves to the right, the rack on its piston rod will not push the gear 37 to move, at this time there is no resistance to the movement of the rack .
  • the pressure sensor senses that the pressure has weakened a lot, and the control part drives the motor 36 to drive the gear 37 to rotate, pushing the rack on the piston assembly that meshes with the gear 37 to the left, pushing the piston cylinder 34
  • the liquid returns to the inside of the resistance member 38.
  • Turning the resistance adjustment cover 50 can drive the one-way valve base 45 to rotate.
  • the top of the one-way valve base 45 is a half-cylindrical surface. When rotating, it can block different numbers of damping holes in the inner tube 44, so the fluid in and out can be adjusted. resistance. In this way, different sizes of resistance are provided to the muscles around the vagina.
  • the liquid inside the resistance member 38 When the liquid inside the resistance member 38 is pushed out of the vagina, the liquid pushes the one-way valve 46, and the fluid passage here is blocked, so the liquid can only be pushed out of the vagina through the above-mentioned damping hole.
  • the check valve 46 When the liquid in the piston cylinder is pushed back, the check valve 46 is pushed down, and the liquid advances the cavity between the inner tube 44 and the inner sleeve 43 through the bar-shaped hole at the bottom of the check valve base 46.
  • the water return operation of the piston assembly 33 can also be manually controlled by the user through another button.
  • the third embodiment shown in FIG. 14 is another case where the present invention is applied to a female pelvic floor muscle exerciser (female health equipment).
  • the basic situation is similar to that of the second embodiment. The difference is that the damper adjustment part and the check valve are moved to the frame.
  • the human contact end assembly 59, the duct 57, the damping adjustment assembly 56, and the check valve 55 are resistance members.
  • the check valve 55 and the damping adjustment component 56 are connected in parallel. One end is connected to the piston cylinder 64 through the conduit 58, and the other end is connected to the human body contact end component 59 through the conduit 57.
  • the air pump 63 is used to inflate the airbag cover 71 of the human body contacting end assembly 59 to inflate it.
  • the liquid crystal screen 65 can display related information such as the liquid pressure, the number of times of exercise, the maximum pressure applied by the user.
  • the pressure sensor is located on the upper end of the damping adjustment component 56. The operation of components such as the air pump 63, the electric motor 69, the damping adjustment assembly 56 (with a stepping motor inside) is controlled by the control unit 66.
  • the airbag jacket should be as thin as possible and the rebound force should be as small as possible.
  • the inflatable layer has only one arc-shaped protrusion, and it can also be made into the shape of several arc-shaped protrusions.
  • the fourth embodiment shown in FIG. 17 is a case where the present invention is applied to a vibrator in the rectum.
  • the balloon 78 is inserted into a closed cavity between the balloon jacket 83 and the inner tube 85 (made of a hard material) through a catheter 79.
  • the battery 80 is installed in the end cover 81, and the eccentric vibration motor 84 is installed inside the inner tube 85.
  • the airbag cover 83 is attached to the outside of the inner tube 85 and is fixed and sealed by the fixing rings 82 and 86.
  • When in use first put a condom cover on the condom, apply lubricating oil, put it in the rectum from the anus, and then repeatedly pinch the airbag 78 to expand the airbag cover 83 in the rectum. After feeling suitable, turn on the motor 84, the whole machine Start vibration massage. It can be used to treat diseases such as semen liquefaction.
  • control circuits switches, wires, power supplies, and control components are not shown in the above figure. These are the tasks that ordinary people in the industry can complete.
  • the shell is also omitted and not shown.

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pain & Pain Management (AREA)
  • Rehabilitation Therapy (AREA)
  • Epidemiology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Reproductive Health (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Biomedical Technology (AREA)
  • Engineering & Computer Science (AREA)
  • Otolaryngology (AREA)
  • Hematology (AREA)
  • Anesthesiology (AREA)
  • Physics & Mathematics (AREA)
  • Biophysics (AREA)
  • Pathology (AREA)
  • Medical Informatics (AREA)
  • Molecular Biology (AREA)
  • Surgery (AREA)
  • Percussion Or Vibration Massage (AREA)

Abstract

一种用于生殖系统的设备，可用于解决女性不孕、男性不育、男性精液不液化、前列腺炎的治疗，女性卵巢、子宫、输卵管、阴道保健、优生优育等领域。它利用流体对女性生殖系统腔道施加交变应力，疏通输卵管堵塞，对子宫、输卵管、卵巢施加变化的压力，达到按摩、保健、治疗的效果。

Description

用于生殖系统的设备 技术领域
本发明涉及一种用于生殖系统的设备，可用于解决女性不孕、男性精液不液化、前列腺炎的治疗，女性卵巢、子宫、输卵管、阴道保健、优生优育等领域。
背景技术
目前有很多女性因为输卵管堵塞、卵巢早衰、子宫问题造成不孕不育。目前这方面的治疗技术主要是用硬质金属丝进行疏通，或采用手术切断堵塞部分、再粘合被切断的残余部分。由于这些方法直接破坏输卵管堵塞处的组织，所以都比较容易造成疏通后再次堵塞。
男性精液不液化的治疗，目前都是靠药物进行，效果甚微。
由于卵巢位于人体较深的位置，难以用普通的按摩器对它进行保健按摩，所以市场上还没有用于卵巢的按摩设备。
发明内容
本发明的目的是提供新型装置和治疗方法，用于解决女性不孕、男性精液不液化、男性不育、前列腺炎以及卵巢、子宫、阴道、输卵管的保健。
本发明的目的是这样实现的：提供一种用于女性生殖系统的设备，它至少由控制零部件、流体激励装置(流体激励装置是指对流体施加压力、改变流体压力的装置)、人体接触端(人体接触端是指和人体接触的零部件)构成，人体接触端可和人体接触，可形成密封的接触面，流体激励装置和人体接触端连接(直接或间接连接，直接连接时，人体接触端直接设置于流体激励装置，间接连接可通过管子连接)，控制零部件和流体激励装置连接，可控制流体激励装置的运行，流体激励装置(直接或间接地)作用于流体，使流体产生压力，流体压力(直接或间接地，正压、负压)作用于人体。接触位置可为女性阴部、阴道、子宫、子宫颈、输卵管、子宫和输卵管相交处等位置及附近。控制零部件最简单的形式是一个电源插头，复杂的则是集成电路。所述的流体可以是气体，也可以是液体。
优选地，上述设备采用电力驱动流体激励装置。
优选地，所述流体可以是气体和液体的组合。子宫内放置含药物的液体，而设备本身可以使用气体或液体。当然，子宫内也可以不用液体，而直接使用气体。
优选地，所述流体和人体可直接接触，没有间隔物。
优选地，所述的流体的压强随时间变化，压强的升降循环进行。
优选地，所述流体激励装置产生的流体压强周期性变化。高频度的压强、压力改变，可以形成对女性生殖系统振动性按摩作用。
所述人体接触端可进入子宫内，和子宫、输卵管接触。
为改进上述方案，所述的人体接触端带有可膨胀的流体空腔，流体充入该空腔后，该空腔膨胀，空腔外部和人体贴合、密封。
为改进上述方案，它具有预充压装置，使生殖系统内部先充满流体，在流体激励装置开始运行之前，处于一定压力之下。
可以在以上技术方案上加上磁体、远红外发热元件等常用保健设备所用零部件。
为了防止压力过大对人体造成伤害，和人体连通的流体管道内可设有安全阀、最大压力调整部件、测压部件。
优选地，该设备带有调节流体压力大小的构件。
优选地，该设备带有手动调节流体压力大小的构件，以确定用户可以承受的最大压力。
优选地，该设备带有频率、流体排量调节装置。
流体激励装置可以是：在弹性流体空腔的弹性壁，安装一个振子(偏心电机等)。也可以安装其它常见流体增压装置或其改装的装置，如各种水泵、气泵。
压力的变化范围可以是负数至正数，也可以是0至正数，也可以是0至负数，或者其它任意数据范围。
如果需要，可以在人体接触端增加固定装置，以便将人体接触端固定在人体上。
人体接触端的分类：
1、覆盖整个女性外阴。外形根据女性外阴形状而定，由软胶材料制成。使用者可以坐在上面，利用自身重力压在弹性材料制成的接触端，从而密封接触端。
2、覆盖阴道口：
l利用自身重量压紧阴道口和接触端。
l使用者仰卧，臀部抬高，阴道口位置高于子宫，便于药水进入子宫和输卵管，此时依靠外力将接触端和阴部压紧，可使用背带或者腰带等固定装修将接触端固定在阴部。
l在阴道口周围，设置一个环形的真空吸附带，通过抽吸真空而密封。
l在阴道入口设置中空的锥形塞(见图7)。
l基于上述的基础，或者不使用上述基础，在进入阴道的部分，内层为硬质空心管，空心管外层安装流体弹性囊，使用之前，流体弹性囊被充入空气或液体膨大，弹性囊四周和阴道压紧贴紧，从而密封。上述弹性囊可以是沿着阴道轴向布置的几个环形气囊。
3、覆盖输卵管或子宫颈入口：
可参考上述密封方式，只是形状、大小做适当调整。进入子宫内部操作的时候，需要相关的内窥镜配合。
上述的技术方案及特征，可应用于优生优育的设备。
上述的技术方案及特征，还可应用于卵巢按摩器、卵巢保健、卵巢功能增强、子宫按摩、阴道按摩等设备。
上述的技术方案及特征，可应用于治疗女性不孕不育的设备，尤其是治疗输卵管堵塞、卵巢功能障碍、子宫内膜太薄等问题。
上述的技术方案及特征，可应用于治疗男性精液不液化、前列腺炎的设备。使用时，该设备的人体接触端被置入直肠内或肛门外。
上述的技术方案及特征，可应用于治疗男性不育的设备。此时人体接触端为一个开口的、可密封的容器，可将男性生殖器官(部分或全部)置于该容器中。阴囊、睾丸等器官可以从开口处进出容器。开口处具有密封零部件，可使开口处和人体接触面密封。
本发明提供了一种治疗女性不孕的方法，利用流体对女性生殖系统腔道施加随时间变化的压力。优选地，所述流体的压强周期性变化。
本发明提供了一种女性保健的方法，利用流体对女性生殖系统腔道施加随时间变化的压力，从而对输卵管、卵巢、子宫等女性生殖器官施加作用力。优选地，所述流体的压强周期性变化。
以上所述的女性生殖系统腔道包括：阴道、子宫颈、子宫、输卵管、卵巢。
本发明提供一种女性保健器械，它至少由一个阻力部件、可膨胀的流体空腔、流体充放装置构成，流体充放装置和可膨胀的流体空腔相连，可将流体充入可膨胀的流体空腔，流体充入该空腔后，该空腔膨胀，空腔外围和人体贴合，阻力部件和可膨胀的流体空腔存在这样的部分，它们在阴道轴向截面同时存在(也就是说，可膨胀的流体空腔和阻力部件并排地置于阴道内或流体空腔将阻力部件包围，而非沿着阴道轴向串联地置于阴道 内)。如果一个弹性容器在没有充入流体的情况下内容积比较小，充入流体后内容积变大了，那么它就是可膨胀的。
为改进上述方案：它带有至少两个独立的空腔，他们相互不联通(通过阀门等装置隔开的仍属于独立的空腔)，其中一个为上述的可膨胀的流体空腔。
为改进上述方案：所述的空腔，至少有一个和阻尼调整装置连通(包括阻尼调整装置位于空腔内的情况，仍属于连通)；另外一个和流体充放装置相连(如手压气囊)。
为改进上述方案：它还带有压力传感器。优选地，压力传感器位于阻尼调整装置和阻力部件的受力处之间。
本发明提供一种女性保健器械，它至少由人体接触端、阻力部件、流体激励部件、控制部件等构成，人体接触端通过阻力部件和流体激励部件连接(阻力部件位于人体接触端内部的情况也属于连接)，控制部件和流体激励部件连接，阻力部件内含有阻尼阀，流体通过阻尼阀进出流体激励部件、人体接触端；控制部件可以控制流体激励部件的运行；流体激励部件可将流体通过阻尼阀压回人体接触端。流体通过阻尼阀被挤出人体接触端的时候产生的阻力可以为女性盆腔内的肌肉收缩提供阻力；流体进入人体接触端后，由女性盆腔内的肌肉收缩后挤压人体接触端，从而将流体通过阻尼阀压出人体接触端。
当以上部件分别独立时，他们之间可用导管连接；如果制为一体时则通过内部的管道连接。
优选地，所述的阻尼阀的阻力大小可调。
优选地，所述的阻尼阀是单向阀，当流体激励部件将流体压回人体接触端时的阻尼较小，反向则较大。
优选地，流体激励部件由电力驱动。
由于经期女性生殖道酸性环境变差，容易造成感染，因此经期内避免使用以上设备。
本发明还提供一种被置于直肠内的设备，它至少由一个振动构件、可膨胀的流体空腔、流体充放装置构成，流体充放装置和可膨胀的流体空腔相连，可将流体充入可膨胀的流体空腔，流体充入该空腔后，该空腔膨胀，空腔外围和人体贴合。
振动构件和可膨胀的流体空腔连接，振动构件和可膨胀的流体空腔存在这样的部分，它们在直肠轴向截面同时存在。
作为改进的方案，上述振动构件安装在一硬质管内，可膨胀的流体空腔安装于硬 质管外，并和流体充放装置连通。
优选地，以上方案都可以带有和手机配套的手机APP，控制相关的设备运行、显示运行参数。当然，也可以通过专门的显示设备显示相关的运行参数。
本文所述部件、组件、零部件、构件等词汇，对其所含的零件数量、关系没有特殊的限制或特别的定义、含义，不局限于机械教科书的概念。本文所述的设备、仪器、装置等概念，对其所含零部件数量、复杂程度并无特别要求，不受教科书概念所限制。
优点
从微观上看，本发明是通过压力的反复变化，使输卵管黏连处反复弯折、复位，在微观上造成黏连处的不同组织(黏连的人体组织、堵塞物和输卵管)疲劳破坏，破损尺寸较小，而逐步脱离。可以通过每天一定时间的使用，通过多天积累逐渐去修复，慢慢破损、慢慢修复，破损处逐渐修复，因此不容易复发黏连。而金属丝直接去捅破黏连组织是一次性强行造成黏连组织断裂，伤口比较大，这样大的伤口在自己修复的时候，两个断裂处很容易再次黏连。
压力的反复变化作用，也使输卵管堵塞处的管壁反复弯折运动，管壁弹性将得到增强、整个输卵管将在压力作用下扩大，更利于卵子、受精卵的运动。
本技术操作方便，患者可以持续通过多天进行渐进的治疗。而金属丝疏通需要复杂的腹腔镜等设备，都是进行一次性疏通就结束。
而通过流体给女性生殖腔道反复施压，对女性的生殖腔道、子宫、输卵管、卵巢都可以起到锻炼作用，有利于提高、加强这些器官的功能，提高所产生卵子的质量，从而达到优生优育的目的。
附图说明
下面结合附图和实施例对本发明作进一步说明。
图1是本发明实施例1装配体的三维立体视图。
图2是本发明实施例1装配体的三维立体透视图。
图3是图2内的组件18的剖视图。
图4是图2内的组件18膨胀后的剖视图。
图5是本发明实施例1所选配的人体接触端的三维剖视图。
图6是本发明实施例1所选配的另一人体接触端的三维剖视图。
图7是本发明实施例1所选配的另一人体接触端的三维剖视图。
图8是本发明实施例2整机装配体的正视透视图。
图9是本发明实施例2整机装配体的三维立体视图。
图10是图8中组件38的剖视图。
图11是图10中组件45的三维立体视图。
图12是图10中组件44的三维立体视图。
图13图8中组件38膨胀后的三维立体视图。
图14是本发明实施例3整机装配体的正视图。
图15是本发明实施例3整机装配体的三维立体剖视图。
图16是图14中组件59的剖视图。
图17是本发明实施例4整机装配体的三维透视图。
图2中：1、导管；2、活塞缸端盖；3、安全阀；4、活塞缸；5、活塞缸端盖；6、活塞组件；7、导杆；8、滑块；9、步进电机组件；10、电机；11、曲柄；12、手轮；13、拖板；14、摆块；16、压力表；17、机架；172、气泵；18、人体接触端组件；
图3中：19、气囊；20、导管；21、端盖；22、气囊基座；23、固定圈；24、内管；25、气囊套；26、固定圈；
图8中：27、压力表；28、气囊；29、导管；30、导管；31、端盖；32、机架；33、活塞组件；34、活塞缸；35、端盖；36、电机；37、齿轮；38、阻力部件；
图10中：39、气囊基座；40、固定圈；41、端盖；42、气囊外套；43、内套；44、内管；45、单向阀基座；46、单向阀；47、固定圈；48、固定圈；49、端盖；50、阻力调整盖；51、套筒；52、导管；53、压力表；54、气囊；
图14中：55、单向阀；56、阻尼调整组件；57、导管；58、导管；59、人体接触端组件；60、机架；61、导管；62、端盖；63、气泵；64、气缸；65、液晶屏；66、控制部件；67、端盖；68、活塞组件；69、电动机；70、齿轮；
图16中：71、气囊套；72、固定圈；73、固定圈；74、内管；75、固定圈；76、气泵基座；77、内套；
图17中：78、气囊；79导管、；80、电池；81、端盖；82、固定圈；83、气囊外套(膨胀状态)；84、偏心振动电机；85、内管；86、固定圈。
具体实施方式
实施例1是本发明治疗女性不孕不育设备的一种实施方式。
图2中，步进电机组件9、电机10、摆块14都安装于拖板13；电机10带动曲柄11转动，曲柄11通过转动副和导杆7配合，导杆7穿过摆块14的孔，因此曲柄11可以带动导杆7摆动。导杆7穿过滑块8，滑块8和活塞组件6的活塞杆右端形成转动副，因而导杆7左右摆动时可以带动活塞组件6左右移动。
拖板13可在机架17上滑动，步进电机组件9上安装有齿轮，该齿轮和机架17上的齿条啮合，因此步进电机组件9可以控制拖板13在机架17上的滑动。拖板13移动后可以改变导杆7的摆幅。因而可以改变活塞缸的单次排气量，从而改变最终压入人体的气流量。气缸4内的气体，通过导管1进入人体接触端组件18，最终进入人体。
通过调整、设定安全阀3的开通压强，就可以设定最终人体内部最大的流体压力，以确保安全。
压力表16和气泵172通过导管接入活塞缸4。压力表16显示活塞缸内的压强，也就是实际施加在人体内的压强。
曲柄11的转动可以由电动机10带动，也可以由摇动手轮12带动，由人手操作手轮12可以慢速推动活塞运动，因此可以用于做细微调整、测试。
气囊19的充放气功能也可由气泵172完成，只要增加相应的导管、阀门、修改控制程序即可。
气囊套25由软质有弹性的材料(如乳胶)制成，可膨胀变形。气囊19(见图3)通过导管20接入气囊基座22的孔，从而和内管24、气囊套25之间的空腔接通。气囊套25被固定圈26固定、密封于内管24一端；另一端被固定圈23固定、密封于气囊基座22外侧。气囊基座22固定于内管24外围。端盖21和内管24固定。端盖21和图2中的导管1连接。
使用步骤：
将拖板13移动至机架17中部，摇动手轮12，将活塞组件移动到最左端(最左端的设计位置应该不超过安全阀3和压力表16的接入位置)，将人体接触端18置入患者阴道内，反复挤压气囊19(见图3，其配套气阀未画出)，将气体压入内管24和气囊外套25之间的流体空腔，气囊外套25膨胀，和阴道贴紧密封。膨胀后的状态见图4。
启动气泵172，向患者体内压入气体，用于施加预加的压力，同时询问患者感受，患者表示不适或有痛感时，停止气泵172，此时压力表16的压强即为患者可以使用的最大压强。
患者可承受的最大压力的确定，也可由人工摇动手轮12来完成。
活塞组件6的往复推动，也可以用推拉式电磁铁、偏心电动机、曲柄滑块结构、或其它常见的能实现直线运动的机械结构完成(具体可参考机械原理方面的书籍)。
调整电机10的转速，即可改变生殖腔道内所受的压力的变化频率。
图5、6、7分别是人体接触端的另外几种形式。其中，图6中右侧顶端的导管可接抽真空的部件，从而形成负压，吸附于人体。
实施例2
图8所示的实施例2是本发明应用于女性盆底肌锻炼器的情况。
使用时，阻力部件38被置入用户阴道内。
压力表27、气囊28通过导管29接入阻力部件38内的空腔。
图10中，气囊外套42由软质材料(如乳胶)制成，有弹性，可膨胀变形。内套也由软质材料(如硅胶)制成，可向内压缩。用手反复挤压气囊54(也就是图8中的气囊28)，将气体压入气囊外套42和内套43之间的密封空腔。实际操作时，通过控制部件将活塞组件33锁死固定，因此在气囊54充气的时候，内套43无法向内压缩。当用户感觉合适的时候，即可停止充气，活塞组件33解锁。图13即为气囊外套42膨胀后的状态。
用户收缩阴道周围的肌肉，将气囊外套42向内压缩，进而压缩内套43，内套43内的液体，通过内管44中部的阻尼孔进入内管44，再经过导管30，进入活塞缸34，推动活塞组件33向右运动，齿轮37内部有单向棘轮，因此当活塞组件33向右运动时，其活塞杆上的齿条并不会推动齿轮37运动，此时齿条的运动没有阻力。当用户松开阴道周围的肌肉时，压力传感器感知到压力减弱很多，控制部件驱动电机36带动齿轮37转动，推动和齿轮37啮合的活塞组件上的齿条向左运动，推动活塞缸34内的液体回到阻力部件38内部。转动阻力调整盖50就可以带动单向阀基座45转动，单向阀基座45顶部为一半圆柱面，转动的时候可以阻挡住内管44上不同数量的阻尼孔，因此可以调节进出的流体阻力。通过这种方式给阴道周围的肌肉提供大小不同的阻力。当阻力部件38内部的液体被推出阴道时，液体推动单向阀46，此处的流体通道被阻断，因此液体只能通过上述的阻尼孔被推出阴道。而当活塞缸内的液体被推回时，单向阀46被压下，液体通过单 向阀基座46底部的条形孔推进内管44和内套43之间的空腔。活塞组件33的回水动作，也可以由用户通过另外的按钮进行手动控制。
实施例3
图14所示的实施例3是本发明应用于女性盆底肌锻炼器(女性保健器械)的另外一种情况。基本情况和实施例2相似。区别在于将阻尼调整部件和单向阀移到机架上。
人体接触端组件59、导管57、阻尼调整组件56、单向阀55即为阻力部件。
单向阀55和阻尼调整组件56并联，一端通过导管58接入活塞缸64，另外一端通过导管57连接到人体接触端组件59。气泵63用于给人体接触端组件59的气囊套71内充气，使其膨胀。液晶屏65可显示用户施加的液体压强、锻炼次数、最大压强等相关信息。压力传感器位于阻尼调整组件56上端。气泵63、电动机69、阻尼调整组件56(内有步进电机)等零部件的运行都受到控制部件66的控制。
以上实施例2和3中，气囊外套应尽量薄，回弹力应尽量小。图中，充气层只有一个弧型凸起，也可以制成几个弧型凸起的形状。
实施例4
图17所示的实施例4是本发明应用于直肠内的振动器的情况。
气囊78通过导管79接入气囊外套83和内管85(硬质材料制成)之间的封闭空腔。电池80安装于端盖81内，偏心振动电机84被安装于内管85内部。气囊外套83安装于内管85外部，被固定圈82、86固定、密封。使用时，先将气囊外套套上避孕套、抹上润滑油，从肛门放入直肠内，然后反复手捏气囊78，使气囊外套83在直肠内膨胀，感觉合适后，开启电机84，整机开始振动按摩。可用于治疗精液不液化等疾病。
为作图简便，以上图中，控制电路、开关、电线、电源、控制部件等常见零部件都没画出，这些都是业内普通人员可以完成的工作。外壳也省略没画出。

Claims (8)

  1. 一种用于女性生殖系统的设备，其特征是：它至少由控制零部件、流体激励装置、人体接触端构成，人体接触端可和人体接触，可形成密封的接触面，流体激励装置和人体接触端连接(直接或间接连接)，控制零部件和流体激励装置连接，控制零部件可控制流体激励装置的运行，流体激励装置(直接或间接地)作用于流体，使流体产生压力，流体压力(直接或间接地)作用于人体，所述的流体的压强随时间变化，压强的升降循环进行。
  2. 如权利要求1所述的用于女性生殖系统的设备，其特征是：所述流体激励装置由电力驱动。
  3. 如权利要求1和2中任一项所述的用于女性生殖系统的设备，其特征是：所述流体可和人体直接接触。
  4. 如权利要求1～3中任一项所述的用于女性生殖系统的设备，其特征是：所述流体激励装置产生的流体压强周期性变化。
  5. 如权利要求1～4中任一项所述的用于女性生殖系统的设备，其特征是：所述的人体接触端带有可膨胀的流体空腔，流体充入该空腔后，该空腔膨胀。
  6. 一种不孕不育治疗仪，其包括如权利要求1～5中任一项所述的用于女性生殖系统的设备。
  7. 一种前列腺治疗仪，其包括如权利要求1～5中任一项所述的用于女性生殖系统的设备。
  8. 一种精液不液化治疗仪，其包括如权利要求1～5中任一项所述的用于女性生殖系统的设备。
PCT/CN2019/105521 2018-09-14 2019-09-12 用于生殖系统的设备 WO2020052616A1 (zh)

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CN2041154U (zh) * 1987-12-12 1989-07-19 姚铁人 妇产科多功能诊断治疗器
US5030202A (en) * 1989-05-12 1991-07-09 Equibov Ltd. Lavage system
GB2260622A (en) * 1991-10-19 1993-04-21 John Gutridge Control of fluid pressure in clinical procedures
CN2439258Y (zh) * 2000-08-28 2001-07-18 赵连三 盆肌生理功能诊疗仪
CN105411561A (zh) * 2015-12-23 2016-03-23 北京君仪凯医疗科技有限公司 一种肛门压力检测和锻炼的康复治疗设备
CN106362232A (zh) * 2016-11-14 2017-02-01 李建魁 一种肛门多功能保健装置
WO2017087455A1 (en) * 2015-11-17 2017-05-26 Previvo Genetics, Inc. Recovery and processing of human embryos formed in vivo

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN2041154U (zh) * 1987-12-12 1989-07-19 姚铁人 妇产科多功能诊断治疗器
US5030202A (en) * 1989-05-12 1991-07-09 Equibov Ltd. Lavage system
GB2260622A (en) * 1991-10-19 1993-04-21 John Gutridge Control of fluid pressure in clinical procedures
CN2439258Y (zh) * 2000-08-28 2001-07-18 赵连三 盆肌生理功能诊疗仪
WO2017087455A1 (en) * 2015-11-17 2017-05-26 Previvo Genetics, Inc. Recovery and processing of human embryos formed in vivo
CN105411561A (zh) * 2015-12-23 2016-03-23 北京君仪凯医疗科技有限公司 一种肛门压力检测和锻炼的康复治疗设备
CN106362232A (zh) * 2016-11-14 2017-02-01 李建魁 一种肛门多功能保健装置

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