Abstract: A penile prosthesis demonstration tool includes a housing having an anterior face and a posterior face, and a male genital tool including a penis tool attached to a scrotum tool, with the male genital tool connected to the anterior face of the housing. An implant including a pump is placed inside of the scrotum tool and an inflatable penile implant placed inside of the penis tool, with the posterior face connected to the housing to secure a reservoir inside of the housing between the anterior face and the posterior face of the housing.

Abstract: An inflatable penile prosthetic system includes a tubing assembly insertable to a penile prosthesis and a pump adapted move liquid out of a reservoir and into the penile prosthesis.

Abstract: A neopenis includes an implant and a support. The implant is an implantable prosthesis that is implantable into a neophallus and adapted to provide the neophallus with an erection. The support is configured for attachment to a ramus of a pelvis. The implantable prosthesis in combination with the support are adapted to orient the neopenis in an anatomically natal penis position that is adapted for penetrative intercourse.

Abstract: An implantable support is provided to secure an implanted prosthesis in a natal male or a trans-male. The implantable support has a base portion attachable to a pelvis, an artificial ligament coupled to the base portion, and an artificial crus penis recess that is sized to receive a proximal end portion of a penile prosthesis. The artificial ligament orients the penile prosthesis within a neopenis anatomically in a position of a natal penis and in a position adapted for penetrative intercourse.

Abstract: A waste collection bag adapted for use by a person having a colostomy, an ileostomy, or a urostomy. The waste collection bag has a rear wall, a front wall on an opposite side of the waste collection bag from the rear wall, and a waste inlet formed in the rear wall of the waste collection bag. The waste inlet sized to fit around a stoma that has been formed through skin of the person. At least the front wall of the waste collection bag has a wall color characterized by a color value measured by a CMYK color code system, where the color value is in a range of: M from 0 to 15; Y from 0 to 10; and K from 10 to 25.

Abstract: An implantable support implantable in a neophallus to support a neopenis includes a first tubular sleeve extending from a proximal end portion to a distal end portion; a first base coupled to the proximal end portion of the first tubular sleeve, where the first base is adapted to be secured to a pubic ramus of a pelvis; and a first opening formed in the first tubular sleeve, where the first opening communicates with a recess that is sized to receive an implantable penile prosthesis. The first tubular sleeve is adapted to provide the neophallus with an artificial tunica located between the recess and the neophallus of the neopenis.

Abstract: In a method and handheld device for capturing and digitally storing images of a wound, stoma, fistula or stoma wafer site, a representation of a view field of an optical lens of a camera is represented at a monitor. A marker is inserted in the representation of the view field in the monitor before an image is stored, the marker being configured to aid a user's positioning of the digital camera relative to the wound area, stoma, fistula or wafer. The patient holds the handheld wound and stoma imaging device in a position relative to his/her own body or in relation to the wafer, while the monitor is simultaneously viewable by the patient. Upon receipt of auser-input for effecting digital storage of the image in the view field, the image is stored in a memory of the handheld wound and stoma imaging device. The device may include a tablet device of smart phone suitably programmed by means of an applet, and optionally an adapter for facilitating the patient's handling of the device.

Abstract: A method of forming a urinary catheter is disclosed that includes injecting a polymer melt through a primary melt channel and into an elongated recess around an outer surface of a core; and controlling a first pressure of the polymer melt in a first secondary melt channel separately and individually from a second pressure of the polymer melt in a second secondary melt channel and reducing stress of the polymer melt along the elongated recess. Opening the mould and removing the core provides a moulded intermittent urinary catheter having an open distal end and a closed proximal tip.

Abstract: An endoscopic instrument provides a flexible three-arm snare structure that is adapted to retrieve stones from a human body.

Abstract: An irrigation system for anal or stomal irrigation includes a tubing system attachable between a reservoir and a catheter. The tubing system has a proximal portion attachable to the reservoir and a distal portion including a distal end that is attachable to the catheter, with the tubing system providing an irrigation flow path from the proximal portion attachable to the reservoir through the distal end attachable to the catheter. A pump is operable to move the liquid through the irrigation flow path to provide the anal or stomal irrigation out of the catheter. A pressure control device is attachable to the distal portion of the tubing system and communicates with the catheter. The pressure control device has a valve that is adapted to limit an irrigation pressure for the anal or stomal irrigation out of the catheter to a value less than a pre-determined pressure threshold.

Abstract: A stiffening device is disclosed that is adapted to cooperate with a flexible kidney stone extractor. The stiffening device includes a tube having a lumen sized to receive a part of flexible kidney stone extractor; a diversion member having a channel that is configured to receive a part of the flexible kidney stone extractor; and a connector coupled between the tube and the diversion member. The connector allows the channel of the diversion member to communicate with the lumen of the tube. A proximal portion of the connector is connected to the diversion member and a distal portion of the connector is connected to the tube.

Abstract: A method and a device are described for an ostomy base plate having a storage configuration as delivered to a user and a use configuration as applied to skin of the user. In the storage configuration, a proximal side of the ostomy base plate is substantially convex, and in the use configuration, the proximal side of the ostomy base plate is substantially concave.

Abstract: An adhesive wafer for an ostomy device, the wafer comprising a first adhesive layer, a backing layer on the distal side of the first adhesive layer, a second skin facing adhesive layer and a hole for accommodating a stoma. Embedded between the adhesive layers is a release layer capable of releasing a neutralizing compound to the peristomal skin.

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 device for extending a penile implant includes a support segment having a tip portion and a receiving segment coupled to a distal end of the penile implant. The receiving segment is configured to rotatably receive a threaded portion to secure the support segment to the penile implant. An extension segment is configured to at least partially surround the threaded portion to extend a length between the tip portion and the penile implant.