WO2024258711A1 - Systèmes de fluide dans un implant corporel - Google Patents

Systèmes de fluide dans un implant corporel Download PDF

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Publication number
WO2024258711A1
WO2024258711A1 PCT/US2024/032602 US2024032602W WO2024258711A1 WO 2024258711 A1 WO2024258711 A1 WO 2024258711A1 US 2024032602 W US2024032602 W US 2024032602W WO 2024258711 A1 WO2024258711 A1 WO 2024258711A1
Authority
WO
WIPO (PCT)
Prior art keywords
implant
coupling
pump assembly
base member
tubular
Prior art date
Legal status (The legal status 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 status listed.)
Ceased
Application number
PCT/US2024/032602
Other languages
English (en)
Inventor
Daniel Walter MYHRA
Daragh NOLAN
Thomas SINNOTT
Sai Sardhak CHINTAMAN
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Boston Scientific Scimed Inc
Original Assignee
Scimed Life Systems Inc
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
Priority claimed from US18/733,271 external-priority patent/US20240415657A1/en
Application filed by Scimed Life Systems Inc filed Critical Scimed Life Systems Inc
Priority to EP24737255.0A priority Critical patent/EP4727487A1/fr
Priority to AU2024302196A priority patent/AU2024302196A1/en
Priority to CN202480039227.9A priority patent/CN121398760A/zh
Publication of WO2024258711A1 publication Critical patent/WO2024258711A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/0004—Closure means for urethra or rectum, i.e. anti-incontinence devices or support slings against pelvic prolapse
    • A61F2/0031—Closure means for urethra or rectum, i.e. anti-incontinence devices or support slings against pelvic prolapse for constricting the lumen; Support slings for the urethra
    • A61F2/0036—Closure means for urethra or rectum, i.e. anti-incontinence devices or support slings against pelvic prolapse for constricting the lumen; Support slings for the urethra implantable
    • A61F2/004—Closure means for urethra or rectum, i.e. anti-incontinence devices or support slings against pelvic prolapse for constricting the lumen; Support slings for the urethra implantable inflatable
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02—Prostheses implantable into the body
    • A61F2/26—Penis implants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2220/00—Fixations or connections for prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
    • A61F2220/0025—Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2220/00—Fixations or connections for prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
    • A61F2220/0025—Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • A61F2220/0033—Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by longitudinally pushing a protrusion into a complementary-shaped recess, e.g. held by friction fit

Definitions

  • This disclosure relates generally to bodily implants and more specifically to bodily implants that include fluid systems and inflatable members.
  • Bodily implants with fluid systems and inflatable members may be placed within a body of a patient for a variety of reasons.
  • one treatment for male erectile dysfunction is the implantation of a penile prosthesis that mechanically erects the penis.
  • some patients phalloplasty patients may receive a penile prosthesis.
  • one treatment for urinary incontinence is the implantation of an artificial urinary sphincter.
  • Such penile prosthesis and artificial urinary sphincters may include an inflatable member or members and a fluid system.
  • an implant includes an inflatable member; a pump assembly, the pump assembly being configured to facilitate a transfer of fluid to and from the inflatable member; a tubular member extending from the pump assembly; a base member coupled to the pump assembly; and a coupling member configured to be disposed such that a portion of the tubular member is disposed between the base member and the coupling member to facilitate a coupling of the tubular member to the pump assembly.
  • the base member includes a projection portion configured to be disposed within a lumen defined by the tubular member.
  • the coupling member is configured to be disposed such that a portion of the coupling member is disposed between the base member and the tubular member.
  • the tubular member extends between the pump assembly and the inflatable member.
  • the implant includes a reservoir configured to store fluid.
  • the implant includes a reservoir configured to store fluid, the tubular member extending between the pump assembly and the reservoir.
  • the base member includes an engagement member
  • the coupling member includes an engagement member configured to engage the engagement member of the base member to couple the coupling member to the base member.
  • the base member defines a cavity, a portion of the coupling member being disposed within the cavity defined by the base member.
  • the base member defines a canty, a portion of the coupling member being disposed within the cavity defined by the base member, a portion of the tubular member being disposed within the cavity defined by the base member.
  • the base member defines a cavity and includes an engagement member extending into the cavity
  • the coupling member includes an engagement member configured to engage the engagement member of the base member to couple the coupling member to the base member.
  • the base member includes an engagement member
  • the coupling member includes a first engagement member and a second engagement member
  • the first engagement member of the coupling member is configured to engage a first portion of the engagement member of the base member
  • the second engagement member of the coupling member is configured to engage a second portion of the engagement member of the base member.
  • the coupling member includes a support portion configured to contact a portion of the tubular member when the tubular member is placed in a non-linear configuration.
  • the coupling member includes a funnel shaped support portion.
  • the coupling member includes a funnel shaped support portion configured to contact a portion of the tubular member when the tubular member is placed in a non-linear configuration.
  • the pump assembly includes a housing having a funnel shaped support portion configured to contact a portion of the tubular member when the tubular member is placed in a non-linear configuration.
  • the implant includes a support member coupled to a portion of the tubular member.
  • a bodily implant includes a housing; a tubular member extending from the housing; a base member coupled to the housing and defining a cavity 7 ; and a coupling member, a portion of the coupling member being configured to be disposed within the cavity defined by the base member.
  • a portion of the tubular member is configured to be disposed within the cavity defined by the base member.
  • the base member includes a projection, at least a portion of the projection being configured to be disposed within a lumen defined by the tubular member.
  • the base member includes an engagement member
  • the coupling member includes an engagement member configured to engage the engagement member of the base member to couple the coupling member to the base member.
  • FIG. 1 schematically illustrates an implant according to an implementation.
  • FIG. 2 illustrates an implant according to an embodiment.
  • FIG. 3 illustrates an implant according to an embodiment.
  • FIG. 4 is a perspective view of a pump assembly according to an implementation.
  • FIGS. 5 and 6 are side views of the pump assembly and a base member.
  • FIGS. 7 and 8 are perspective views of the pump assembly, the base member, and a tubular member.
  • FIGS. 9 and 10 are perspective views of the pump assembly, the base member, the tubular member, and a coupling member.
  • FIGS. 11 and 12 are cross-sectional views of the pump assembly, the base member, the tubular member, and the coupling member.
  • FIG. 13 is an exploded view of the pump assembly, the base member, the tubular member, and the coupling member.
  • FIGS. 14 and 15 illustrate the base member, the tubular member, and the coupling member.
  • FIGS. 16-21 illustrate a pump assembly, a base member, a tubular member, and a coupling member according to another implementation.
  • FIGS. 22-24 illustrate a pump assembly, a base member, a tubular member, and a coupling member according to another implementation.
  • FIGS. 25-28 illustrate a pump assembly, a base member, a tubular member, and a coupling member according to another implementation.
  • the terms “a” or '‘an,” as used herein, are defined as one or more than one.
  • the term “another,” as used herein, is defined as at least a second or more.
  • the terms “including” and/or “having”, as used herein, are defined as comprising (i.e., open transition).
  • the term “coupled” or “moveably coupled.” as used herein, is defined as connected, although not necessarily directly and mechanically.
  • the embodiments are directed to medical devices such as penile prostheses, artificial sphincters, or other bodily implants.
  • the term patient or user may hereafter be used for a person who benefits from the medical device or the methods disclosed in the present disclosure.
  • the patient can be a person whose body is implanted with the medical device or the method disclosed for operating the medical device by the present disclosure.
  • the patient may be a human male, a human female, or any other mammal.
  • the embodiments discussed herein may improve the performance of a bodily implant.
  • the bodily implant may have improved reliability’ or improved implantation procedures.
  • FIG. 1 schematically illustrates a bodily implant 100 according to an embodiment.
  • the bodily implant 100 may be a penile implant.
  • the bodily implant 100 may be an artificial urinary sphincter.
  • the bodily implant 100 is a different type of bodily implant.
  • the illustrated embodiment includes a pump assembly 110, an inflatable member 190, and a reservoir 195.
  • the pump assembly 110 is operatively and fluidically coupled to the reservoir 195 via tubular member 170.
  • the pump assembly 110 is operatively and fluidically coupled to the reservoir 195 via the tubular member 180.
  • the reservoir 195 is configured to hold or store a fluid.
  • the pump assembly 110 is configured to move fluid from the reservoir 195 to the inflatable member 190 and from the inflatable member 190 to the reservoir 195.
  • the pump assembly 110 may include electronic pump components or manual pump components.
  • the inflatable member 190 is configured to be placed in an inflated state or configuration and in a deflated state or configuration. In some embodiments, the inflatable member 190 is configured to place pressure on a portion of the body when the inflatable member 190 is in the inflated state or configuration.
  • the tubular member 170 is coupled to and extends between the pump assembly 110 and the inflatable member 190.
  • the tubular member 170 is configured to convey fluid between the pump assembly 110 and the inflatable member 190.
  • the bodily implant 100 includes a base member 130 and a coupling member 120.
  • the base member 130 is configured to be coupled to the pump assembly 110, such as to a housing or a surface of the pump assembly 110.
  • the coupling member 120 is configured to engage the base member 130 to help couple the tubular member 170 to the pump assembly 110.
  • the tubular member 180 is coupled to and extends between the pump assembly 1 10 and to the reservoir 195.
  • the tubular member 180 is configured to convey fluid between the pump assembly 110 and the reservoir 195.
  • the bodily implant 100 includes a base member 131 and a coupling member 121.
  • the base member 131 is configured to be coupled to the pump assembly 110, such as to a housing or a surface of the pump assembly 110.
  • the coupling member 121 is configured to engage the base member 131 to help couple the tubular member 180 to the pump assembly 110.
  • the bodily implant 100 may be placed within the body of a patient.
  • the inflatable member 190 may be placed such that it is able to place pressure on a portion of the body of the patient when the inflatable member 190 is in the inflated or expanded configuration.
  • FIG. 2 illustrates a bodily implant 200 according to an embodiment.
  • the implant 200 is an artificial urinary sphincter.
  • the implant 200 includes a pump assembly 210, an inflatable member 290, and a reservoir 295.
  • the pump assembly 210 is operatively and fluidically coupled to the inflatable member 290 via tubular member 270.
  • the pump assembly 210 is operatively and fluidically coupled to the reservoir 295 via the tubular member 280.
  • the reservoir 295 is configured to hold or store a fluid.
  • the pump assembly 210 is configured to move fluid from the reservoir 295 to the inflatable member 290 and from the inflatable member 290 to the reservoir 295.
  • the pump assembly 210 may include electronic pump components or manual pump components.
  • the inflatable member 290 is configured to be placed in an inflated state or configuration and in a deflated state or configuration. In some embodiments, the inflatable member 290 is configured to place pressure on a portion of the body when the inflatable member 290 is in the inflated state or configuration.
  • the tubular member 270 is coupled to and extends between the pump assembly 210 and the inflatable member 290.
  • the tubular member 270 is configured to convey fluid between the pump assembly 210 and the inflatable member 290.
  • bodily implant 200 includes a base member and a coupling member.
  • the base member is configured to be coupled to the pump assembly 210, such as to a housing or a surface of the pump assembly 210.
  • the coupling member is configured to engage the base member to help couple the tubular member 270 to the pump assembly 210.
  • the tubular member 280 is coupled to and extends between the pump assembly 210 and the reservoir 295.
  • the tubular member 280 is configured to convey fluid between the pump assembly 210 and the reservoir 295.
  • bodily implant 200 includes a second base member and a second coupling member.
  • the second base member is configured to be coupled to the pump assembly 210, such as to a housing or a surface of the pump assembly 210.
  • the second coupling member is configured to engage the second base member to help couple the tubular member 280 to the pump assembly 210.
  • FIG. 3 illustrates a bodily implant 300 according to an embodiment.
  • the implant 300 is penile implant.
  • the implant 300 includes a pump assembly 310. an inflatable member 390, and a reservoir 395.
  • the implant also includes a second inflatable member 390 A.
  • the pump assembly 310 is operatively and fluidically coupled to the inflatable member 390A via tubular member 370A.
  • the pump assembly 310 is operatively and fluidically coupled to the inflatable member 390 via tubular member 370.
  • a tubular member with a single end coupled to the pump assembly may couple the pump assembly to both inflatable members (such as a tubular member that includes a second branch or has a Y shape).
  • the pump assembly 310 is operatively and fluidically coupled to the reservoir 395 via the tubular member 380.
  • the reservoir 395 is configured to hold or store a fluid.
  • the pump assembly 310 is configured to move fluid from the reservoir 395 to the inflatable members 390 and 390A and from the inflatable members 390 and 390A to the reservoir 395.
  • the pump assembly 310 may include electronic pump components or manual pump components.
  • the inflatable members 390 and 390A are configured to be placed in inflated states or configurations and in deflated states or configurations. In some embodiments, the inflatable members 390 and 390A are configured to place pressure on a portion of the body when the inflatable members 390 and 390A are in the inflated states or configurations.
  • the tubular member 370 is coupled to the pump assembly 310 and to the inflatable member 390.
  • the tubular member 370 is configured to convey fluid between the pump assembly 310 and the inflatable member 390.
  • bodily implant 300 includes a base member and a coupling member.
  • the base member is configured to be coupled to the pump assembly 310, such as to a housing or a surface of the pump assembly 310.
  • the coupling member is configured to engage the base member to help couple the tubular member 370 to the pump assembly 310.
  • the tubular member 370A is coupled to the pump assembly 310 and to the inflatable member 390A.
  • the tubular member 370A is configured to convey fluid between the pump assembly 310 and the inflatable member 390 A.
  • bodily implant 300 includes a base member and a coupling member.
  • the base member is configured to be coupled to the pump assembly 310, such as to a housing or a surface of the pump assembly 310.
  • the coupling member is configured to engage the base member to help couple the tubular member 370A to the pump assembly 310.
  • the tubular member 380 is coupled to the pump assembly 310 and to the reservoir 395.
  • the tubular member 380 is configured to convey fluid between the pump assembly 310 and the reservoir 395.
  • bodily implant 300 includes a base member and a coupling member.
  • the base member is configured to be coupled to the pump assembly 310, such as to a housing or a surface of the pump assembly 310.
  • the coupling member is configured to engage the base member to help couple the tubular member 380 to the pump assembly 310.
  • FIGS. 4-15 illustrate a pump assembly 410, a base member 430, a tubular member 490, and a coupling member 420 according to an implementation.
  • FIG. 13 is an exploded view of the implementation.
  • the tubular member 490 may be used to fluidically couple the pump assembly 410 to an inflatable member or to a fluid reservoir.
  • the bodily implant may include several tubular members that fluidically couple the pump assembly to other components, such as a fluid reservoir or an inflatable member. While only one tubular member 490 and its coupling to the pump assembly 410 is illustrated and described in detail, it should be understood that such a coupling may be used to couple other or more than one tubular member to the pump assembly or to other portions or components of the device.
  • the pump assembly includes a housing 412.
  • the base member 430 is coupled to the housing 412 of the pump assembly 410 within a recess 414 defined by the housing 412.
  • the base member 430 may be coupled to a surface of the housing, such as a non-recessed outer surface of the housing.
  • the housing 412 and the base member 430 are formed of metal and the base member 430 is coupled to the housing 412 via a welding, such as a laser welding, process.
  • the base member or the housing or both are made of different materials.
  • the base member is coupled to the housing via a different coupling mechanism, such as an adhesive.
  • the housing and the base member may be unitarily or monolithically formed. In such an implementation, the housing may be formed or machined to have the structure and form of the housing and the base member when the base member is coupled to the housing.
  • the recess is in communication with a lumen or opening 416 defined in the housing 412.
  • the lumen or opening 416 is in communication with pumps and valves within the pump assembly to facilitate fluid flow to and from the pump assembly via that lumen or opening 416.
  • the base member 430 includes a projection 432.
  • the projection 432 defines a lumen 433.
  • the lumen 433 defined by the base member 430 is in fluid communication with the lumen or opening 416 defined by the housing 412.
  • the tubular member 490 may be placed over the projection 432 of the base member 430.
  • the projection 432 of the base member 430. or a portion of the projection 432 of the base member 430 extends into a lumen 492 defined by the tubular member 490.
  • the tubular member 490 is a kink resistant tubing.
  • the tubular member is a different ty pe of member or is formed of different materials.
  • the coupling member 420 is moved or slid along an outer surface of the tubular member 490.
  • the coupling member 420 defines a lumen 422.
  • the tubular member 490 is disposed within the lumen 422.
  • the coupling member 420 may be moved towards the pump assembly 410 until the coupling member 420 engages the base member 430.
  • base member 430, the coupling member 420, and the tubular member 490 are disposed such that a portion of the coupling member 420 is disposed between a portion of the tubular member 490 and a portion of the base member 430. Additionally, a portion of the tubular member 490 is disposed between a portion of the projection 432 of the base member 430 and a portion of the coupling member 420. In the illustrated implementation, the tubular member 490 is thereby coupled to the pump assembly 410 or the housing 412 of the pump assembly 410.
  • the coupling member 420 is configured to engage the base member 430 and couple to the base member 430.
  • an inner surface 434 of the base member 430 includes a projection or coupling portion 436.
  • the projection or coupling portion 436 of the base member 430 is configured to engage a projection or coupling portion 426 of an outer surface 424 of the coupling member 420 to couple the coupling member 420 to the base member 430.
  • the coupling member may include more than one projection or coupling portion.
  • the base member may include more than one projection or coupling portion.
  • the coupling member attaches or couples to the base member via a different mechanism.
  • the coupling member 420 and the base member 430 are formed of biocompatible materials, such as a polymer material. In some implementations, the materials that form the coupling member 420 and the base member 430 allow the members to be fixedly coupled to each other.
  • FIG. 13 is an exploded view of the components.
  • FIGS. 14 and 15 illustrate the coupler 420 coupled to the base member 430 and to the tubular member 490.
  • FIGS. 16-21 illustrate a coupling member 520 according to an implementation.
  • the coupling member includes a curved or flared surface 528.
  • the curved or flared surface 528 is configured to contact the tubular member 490, such as an outer surface 498 of the tubular member.
  • the curved or flared surface 528 is configured to contact the outer surface 498 of the tubular member 490 when the tubular member 490 is curved or bent into a non-linear configuration to provide support to the tubular member 490.
  • the curved or flared surface 528 may be configured to help prevent the tubular member 490 from becoming kinked or broken.
  • FIGS. 22-24 illustrate a housing 612 of a pump assembly 610 according to an implementation.
  • the housing 612 includes a curved or flared surface 618.
  • the curved or flared surface 618 is configured to contact the tubular member 490, such as an outer surface 498 of the tubular member.
  • the curved or flared surface 618 is configured to contact the outer surface 498 of the tubular member 490 when the tubular member 490 is curved or bent into a non-linear configuration to provide support to the tubular member 490.
  • the curved or flared surface 618 may be configured to help prevent the tubular member 490 from becoming kinked or broken.
  • FIGS. 25-28 illustrate a system according to another implementation.
  • the system includes a support member 750.
  • the support member 750 is configured to contact the tubular member to provide support to the tubular member.
  • the support member 750 may be configured to help prevent the tubular member from becoming kinked or broken.
  • the support member 750 fits over or is coupled to two tubular members and is disposed on top of the pump assembly housing. In implementations, the support member may be located at a different location along the tubular member.

Landscapes

  • Health & Medical Sciences (AREA)
  • Vascular Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Oral & Maxillofacial Surgery (AREA)
  • Transplantation (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Cardiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Animal Behavior & Ethology (AREA)
  • Urology & Nephrology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Reproductive Health (AREA)
  • Prostheses (AREA)

Abstract

Selon un aspect, un implant (100) comprend un élément gonflable (190) ; un ensemble pompe (110), l'ensemble pompe étant conçu pour faciliter un transfert de fluide vers et depuis l'élément gonflable ; un élément tubulaire (170) s'étendant à partir de l'ensemble pompe ; un élément de base (130) raccordé à l'ensemble pompe ; et un élément de raccordement (120) conçu pour être disposé de telle sorte qu'une partie de l'élément tubulaire est disposée entre l'élément de base et l'élément de raccordement pour faciliter un raccordement de l'élément tubulaire à l'ensemble pompe.
PCT/US2024/032602 2023-06-13 2024-06-05 Systèmes de fluide dans un implant corporel Ceased WO2024258711A1 (fr)

Priority Applications (3)

Application Number Priority Date Filing Date Title
EP24737255.0A EP4727487A1 (fr) 2023-06-13 2024-06-05 Systèmes de fluide dans un implant corporel
AU2024302196A AU2024302196A1 (en) 2023-06-13 2024-06-05 Fluid systems in a bodily implant
CN202480039227.9A CN121398760A (zh) 2023-06-13 2024-06-05 身体植入物中的流体系统

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US202363507868P 2023-06-13 2023-06-13
US63/507,868 2023-06-13
US18/733,271 US20240415657A1 (en) 2023-06-13 2024-06-04 Fluid systems in a bodily implant
US18/733,271 2024-06-04

Publications (1)

Publication Number Publication Date
WO2024258711A1 true WO2024258711A1 (fr) 2024-12-19

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ID=91738119

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2024/032602 Ceased WO2024258711A1 (fr) 2023-06-13 2024-06-05 Systèmes de fluide dans un implant corporel

Country Status (4)

Country Link
EP (1) EP4727487A1 (fr)
CN (1) CN121398760A (fr)
AU (1) AU2024302196A1 (fr)
WO (1) WO2024258711A1 (fr)

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050137614A1 (en) * 2003-10-08 2005-06-23 Porter Christopher H. System and method for connecting implanted conduits
US8241203B2 (en) * 2010-02-12 2012-08-14 Fogarty Terence M Inflatable penile prosthesis with spool valve
EP3384875A1 (fr) * 2017-04-05 2018-10-10 Coloplast A/S Implant pénien avec tube réglable en longueur
WO2022082194A1 (fr) * 2020-10-15 2022-04-21 Boston Scientific Scimed, Inc. Prothèse pénienne gonflable comprenant un ensemble pompe et procédé de fabrication
WO2024040153A1 (fr) * 2022-08-18 2024-02-22 Boston Scientific Scimed, Inc. Implants corporels avec systèmes de fluide

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050137614A1 (en) * 2003-10-08 2005-06-23 Porter Christopher H. System and method for connecting implanted conduits
US8241203B2 (en) * 2010-02-12 2012-08-14 Fogarty Terence M Inflatable penile prosthesis with spool valve
EP3384875A1 (fr) * 2017-04-05 2018-10-10 Coloplast A/S Implant pénien avec tube réglable en longueur
WO2022082194A1 (fr) * 2020-10-15 2022-04-21 Boston Scientific Scimed, Inc. Prothèse pénienne gonflable comprenant un ensemble pompe et procédé de fabrication
WO2024040153A1 (fr) * 2022-08-18 2024-02-22 Boston Scientific Scimed, Inc. Implants corporels avec systèmes de fluide

Also Published As

Publication number Publication date
CN121398760A (zh) 2026-01-23
EP4727487A1 (fr) 2026-04-22
AU2024302196A1 (en) 2026-01-15

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