Abstract: A method of implanting a penile prosthetic in a patient includes opening a proximal space inside of a crus penis and a distal space inside of an external portion of a penis of the patient. An implantable penile prosthetic is provided having a cylinder and a base, with the base adapted to be coupled to a reservoir and a pump and including an inflatable bladder. Inflation of the inflatable bladder of the base with liquid from the reservoir expands an outer diameter of the base to stabilize the implantable penile prosthetic within the penis of the patient.

Abstract: An anal irrigation system including a control unit (2) is provided. The control unit (2) is connected to an external tube (4) by an extension cord (9), so that pivoting of the control unit (2) with respect to the external tube (4) is possible.

Abstract: A suture assembly includes a leader attached to a suture. The leader includes a band, a clasp extending from a distal edge of the band, and at least two prongs extending from a proximal edge of the band. The band is curved to provide the leader with an exterior surface that defines an outermost perimeter of the leader and an interior surface opposite of the exterior surface. The clasp is crimped onto the suture such that the suture is captured within the outermost perimeter of the leader.

Abstract: An assembly comprising a catheter package, a catheter and a collecting bag is provided. The assembly has means for preventing flow of liquid through the catheter during storage. A sealing element closing the eyelets is provided. An extended cone-lock in a telescopic catheter is also provided.

Abstract: Disclosed is an adaptable ostomy base plate comprising a flexible top film (1), at least one elastic adhesive disposed on the top film and at least one release liner, the base plate having at least a first convex section that can be inverted to a concave section to be used for especially demanding skin surface conditions, such as in ostomists suffering from hernia.

Abstract: Disclosed is a snare instrument with a shaft area, a snare structure in a snaring area distally adjoining the shaft area, and a plurality of noose wires. The snare structure can be pulled closed, from an opened position with distally open snare, and has a plurality of flexible bending tubes which extend distally forwards and radially outwards in a radiating shape to form the snare, and of which the distal ends can be moved radially inwards towards each other so as to pull the snare structure closed. Each noose wire extends with a first base portion from the shaft area loosely through one of the bending tubes as far as the distal end thereof, from there with a noose arch to the distal end of the same or another bending tube, and from there with a second base portion loosely through the latter back to the shaft area. At least one of the noose wire base portions extends through each bending tube.

Abstract: A Wound Moisture and Assessment System includes a flexible coupon containing one or more electrochemical moisture sensors for measuring a moisture profile of a wound. The coupon is activated by a wireless RF scanner that provides power to the coupon for taking moisture measurements, receives the moisture measurements therefrom, and transmits the measurements to a computing device. The moisture measurements can be represented as a wound moisture map that allows a patient or caregiver to assess the health and healing progress of a wound such as an ulcer.

Abstract: Disclosed is a base plate 1 for an ostomy collection device, comprising a cover layer 2 whereon an adhesive layer 3 is at least partly disposed. Immediately surrounding a through-going hole 6, the base plate has an inner area wherein the cover layer extends beyond the adhesive layer in a radial direction toward the through-going hole, thereby providing an overlap 7 protecting the adhesive material from contact with stomal output.

Abstract: A valve insertable into a body lumen includes a body region extending in a distal direction away from a proximal rim. The proximal rim defines an outer perimeter of the valve at a proximal end of the valve. The body region forms a first leaflet and a second leaflet, with the first leaflet in contact with the second leaflet to provide the valve with a closed position. The first leaflet includes a first segment in contact with the proximal rim and a second segment in contact with the second leaflet. The first segment is curved to include a convex exterior surface and a concave interior surface of the valve. The second segment is curved to include a concave exterior surface and a convex interior surface of the valve.

Abstract: An expandable collecting bag is provided. The collecting bag can be used in an ostomy appliance and has a cap portion and an expandable portion. The expandable portion is folded inside the cap portion with the outer surfaces facing each other. The cap portion is folded over and envelopes the expandable portion with the inner surfaces facing each other. A method for producing a collecting bag is also provided.

Abstract: Thermoresponsive skin barrier assemblies are disclosed. One such wound treatment assembly includes a pump configured to expel a biosealant to a pump output port when subjected to a thermal stimulus, and an adhesive substrate layer for covering the wound. The adhesive substrate layer includes a conduit configured to transport the biosealant from the output port to the wound. The assembly further includes a control module in signal communication with a wound leakage sensor configured to activate a heating element disposed in proximity to the pump when wound leakage is detected.

Abstract: An adhesive wafer (10) for an ostomy device, the wafer comprising a skin-facing adhesive layer (40), a backing layer (30) on the non-skin-facing side of the adhesive layer, and a hole (60) for accommodating a stoma. On the central portion of the backing layer is located a release layer (110) being configured to release a neutralizer. The neutralizer is capable of neutralizing or at least minimizing the level of skin or adhesive aggressiveness of the output.

Abstract: A method for treating urinary incontinence includes making a vaginal incision in a patient, and positioning a tape under the urethra through the incision such that one portion of the tape extends from under the urethra and diverts away from the bladder and other vital organs. In one embodiment, once positioned within the patient, the tape adopts a V-shape and provides support for the urethra without altering the position of the urethra.

Abstract: A penile prosthesis kit of parts includes an inflatable implant, a reservoir adapted to contain a volume of liquid, a pump, tubing and tubing connectors provided for attachment of the inflatable implant and the reservoir to the pump, and instructions for use provided for implantation and use of the pump. The pump has a rotary valve located in a first flow path entering into the pump and in a second flow path exiting from the pump. When implanted, the rotary valve is constrained to rotate in only one direction to move a portion of the volume of the liquid from the reservoir through the first flow path and through the second flow path into the inflatable implant.

Abstract: A one-piece or two-piece ostomy appliance comprising a base plate (1), the base plate comprising an adhesive wafer (11) that comprises a top film (8) and at least one skin-friendly adhesive (9) on a proximal surface thereof, for attaching the base plate to the skin of a user, and a first through-going-hole (5). Further, a convex element (10) is arranged distal to a user-interface of the adhesive wafer and has a second through-going hole (15) of the same diameter as the first through-going hole and being co-axially arranged therewith. The convex element comprises a material which reacts to moisture.

Abstract: A suture assembly includes a suture clip connected to a suture. The suture clip includes a proximal end opposite a distal end, a first side edge opposite a second side edge, with each of the first side edge and the second side edge extending from the proximal end to the distal end of the suture clip. The suture clip is formed such that the first side edge is spaced apart from the second side edge to provide an open slot that is adapted to allow the suture clip to flex in a radial direction. A tab extends from the distal end of the suture clip and is crimped to the suture. A rib formed on an interior surface of the suture clip.

Abstract: A urinary catheter assembly (1) for relieving urinary retention is provided, which comprises a package (3) housing a protective sleeve (5) and a catheter (7), the protective sleeve protecting the catheter. To allow a catheter to be removed from the package with or without a protective sleeve, the catheter assembly forms a removal structure configured for at least a first removal procedure and a second removal procedure. The first removal procedure provides simultaneous removal of the catheter and the protective sleeve from the package with the protective sleeve protecting the catheter, and the second removal procedure provides removal of the catheter from the package and retains the protective sleeve in the package.

Abstract: The present invention relates to a method for the preparation of a medical device element by means of extrusion or injection molding and to medical devices comprising such extruded or injection molded medical device elements. The medical device elements (e.g. tubes, wires, lines, stents, catheters, guides, endodontic instruments, needles, trocars for e.g. laparoscopic surgery, laparoscopic accessories, surgical instruments, guide wires) are characterized by a prefabricated shaped article or a thermoplastic substrate polymer having thereon a layer of a covalently cross-linked coating composition of a thermoplastic matrix polymer and a hydrophilic polymer. The method involves a coating composition comprising a thermoplastic matrix polymer, a hydrophilic polymer, and one or more photo-initiator(s), e.g. covalently linked to molecules of the thermoplastic matrix polymer and/or to molecules of the hydrophilic polymer.

Abstract: An ostomy appliance includes a filter construction coupled to an ostomy bag. The filter construction has a pre-filter defined by an outside perimeter, a first cut-out formed through the pre-filter and a separate second cut-out formed through the pre-filter with the second cut-out separated from the first cut-out by a portion of the pre-filter. A deodorizing filter is inserted into the first cut-out.