[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

WO2020052616A1 - Dispositif pour système reproducteur - Google Patents

Dispositif pour système reproducteur Download PDF

Info

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
Authority
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)
Chinese (zh)
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/fr

Links

Images

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.

Landscapes

  • 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

L'invention concerne un dispositif pour un système reproducteur, destiné à être utilisé dans le traitement de l'infertilité féminine et de l'infertilité masculine, de la non-liquéfaction de sperme et de la prostatite, et destiné à être utilisé dans les domaines tels que les ovaires, les utérus, les trompes de Fallope, les soins de santé vaginaux, et la grossesse saine et l'éducation scientifique. Le dispositif applique une contrainte alternative sur une lumière d'un système reproducteur féminin à l'aide d'un liquide pour recanaliser les trompes de Fallope obstruées, et applique des pressions variables sur les utérus, les trompes de Fallope et les ovaires pour obtenir des effets de massage, de soins de santé et de traitement.
PCT/CN2019/105521 2018-09-14 2019-09-12 Dispositif pour système reproducteur WO2020052616A1 (fr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
CN201811075607.0 2018-09-14
CN201811075607 2018-09-14
CN201811198752.8 2018-10-15
CN201811198752 2018-10-15

Publications (1)

Publication Number Publication Date
WO2020052616A1 true WO2020052616A1 (fr) 2020-03-19

Family

ID=69778203

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/CN2019/105521 WO2020052616A1 (fr) 2018-09-14 2019-09-12 Dispositif pour système reproducteur

Country Status (2)

Country Link
CN (1) CN110897853A (fr)
WO (1) WO2020052616A1 (fr)

Citations (7)

* 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
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 (fr) * 2015-11-17 2017-05-26 Previvo Genetics, Inc. Récupération et traitement d'embryons humains formés in vivo

Patent Citations (7)

* 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 (fr) * 2015-11-17 2017-05-26 Previvo Genetics, Inc. Récupération et traitement d'embryons humains formés 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

Also Published As

Publication number Publication date
CN110897853A (zh) 2020-03-24

Similar Documents

Publication Publication Date Title
US3752150A (en) Exercising apparatus
AU2019201070A1 (en) Stimulation device
US20030087734A1 (en) Vaginal-pelvic muscle exerciser and birthing trainer
US20180185641A1 (en) Pelvic muscle exerciser
KR101234768B1 (ko) 발기보조기기
KR20010006356A (ko) 출산을 준비하게 하여 이를 촉진시키는 장치 및 준비 체조
JP2006511280A (ja) 女性刺激装置
US20050234292A1 (en) Hydraulically driven vibrating massagers
US20180318085A1 (en) Inflatable penile prosthesis with pump bulb
US20050049453A1 (en) Hydraulically driven vibrating massagers
GB2352181A (en) Inflatable pessary
US20060200187A1 (en) Childbirth inflatable water/air vaginal obturator
WO2020052616A1 (fr) Dispositif pour système reproducteur
CN201353368Y (zh) 直肠给药装置
US20170150992A1 (en) Prosthetic Artificial Insemination Device
CN204863261U (zh) 一种触诊探头保护套
CN112530261A (zh) 一种可用于远程诊疗男女性功能疾病的仿真ai生殖器结构
CN211273075U (zh) 子宫颈扩张装置
WO2014162363A1 (fr) Outil de soutien intravaginal et dispositif d'injection de fluide
CN204890306U (zh) 充气式子宫托
CN207575292U (zh) 一种组织压缩装置
RU2364380C2 (ru) Презерватив
CN109427232A (zh) 仿生女性生殖器
CN2197016Y (zh) 手动式取精器
CN2201072Y (zh) 可膨胀阴茎假体

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 19860866

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 19860866

Country of ref document: EP

Kind code of ref document: A1