Abstract: The present invention is a drainable ostomy pouch having a closure system that includes a resealable press and seal material. The material facilitates closing and opening of the ostomy pouch outlet. A space between the comfort panel and the pouch material can accommodate the closure system or at least a portion of the closure system.

Abstract: A spring-loaded bag connector having a spring-loaded valve and a housing comprising a fluid inlet portion and a fluid outlet portion. The spring-loaded bag connector is configured to connect with a fluid collection bag to generate a self-closing collection bag. Additionally, the spring-loaded bag connector is configured to couple with a second coupling element, such as a coupling connector, to facilitate the drainage and collection of waste to a fluid collection bag. Uncoupling of the bag connector and the second coupling element results in minimal fluid contamination on the outer surfaces of the bag connector system. The bag connector systems provided herein are included in medical appliances for body waste management.

Abstract: Ostomy appliances with a filter system that is resistant to clogging by waste expelled by the stoma are provided for waste management.

Abstract: Disclosed herein are methods and devices for coupling and securing a medical device appliance. In particular, one piece moldable adhesive structures are disclosed which allow customization of an attachment wafer to the size and shape of, for example, a stoma, while allowing flexibility and security for attaching a medical device, such as an ostomy pouch or other device to the subject.

Abstract: An ostomy appliance including an ostomy pouch with a filter and a center pleated panel to protect the filter, facilitate deodorization and deter ballooning.

Abstract: A fecal catheter or ostomy pouch made of an odor barrier material including a thermoplastic elastomer, odor barrier modifier and an antiblocking agent.

Abstract: A coupling assembly for fastening an adhesive wafer to an ostomy appliance device, the coupling assembly including a captive connection between the adhesive wafer and ostomy appliance that permits captive relative displacement between the entire adhesive wafer and the entrance aperture of the appliance, to facilitate access to the wafer from the non-body-contacting side. The coupling assembly further comprises a fixation coupling for fixing the adhesive wafer in the operative position.

Abstract: A stoma extender includes a first end for insertion into a stoma for diverting stomal effluent into the stoma extender before the effluent exits the stoma; a second end for remaining external of the stoma, for providing a discharge exit for stomal effluent; and a conduit portion coupled between the first and second ends for communicating stomal effluent through the stoma extender, wherein the length of the conduit portion is adjustable stably, to permit adaptation of the stoma extender to an individual's stoma.

Abstract: Disclosed are computer-based systems and media for providing an interactive ostomy treatment guide, and methods of using the same, the guide comprising: a software module configured to receive ostomy assessment information, the assessment information comprising one or more of: condition of skin adjacent an ostomy, topographical location of any peristomal lesion, stoma type, pouching surface type, stoma devices present, and stoma complications; a software module configured to apply a treatment algorithm to the ostomy assessment information to generate an output; and a software module configured to display one or more ostomy management options based on the output.

Abstract: A wound dressing having anti-microbial activity comprises a first fiber capable of bonding with silver (1) cations. The wound dressing comprises a blend of the first fiber to which silver (1) cations are bonded and a second fiber which is substantially free from silver. The wound dressing comprises from 0.01 to 5.0 percent by weight of silver (1) cations, based on the weight of fiber.

Abstract: A controlled discharge ostomy appliance assembly comprises (i) a stoma seal that is self-urging with a dynamic damping characteristic that resists changes of seal volume, (ii) a press-fit coupling member displaceable from an unlocked position to a locked position as part of a press-fit process, and (iii) a single-use frangible portion. The assembly further includes a protector shield removably fastened to the appliance forming a combined assembly therewith. The protector shield comprises (i) a seal displacer manipulable for displacing the stoma seal to a non-operative position ready for fitting, (ii) a substantially rigid coupling member guard portion for protecting the state of the coupling member, and (iii) a bracing portion for bracing the single-use frangible portion.

Abstract: The present invention relates to a valve system for an inflatable portion of an indwelling medical device and more particularly to a valve system for fluid regulation of a catheter comprising a fluid inflatable portion that undergoes pressure changes within the body during use.

Abstract: The present invention relates to an antimicrobial composition suitable for use on skin and wounds comprising a source of an antimicrobial metal ion and a quaternary cationic surfactant.

Abstract: A bag connector system includes a first coupling element, with a self-closing seal and a housing having a fluid inlet port and a fluid outlet port, and a second coupling element, with a housing having a fluid inlet end and a fluid outlet end. The fluid inlet end is configured to displace the self-closing seal when inserted into the fluid outlet port of the first coupling element. A bag connector system optionally includes a locking mechanism to maintain the first coupling element and second coupling element in a coupled state. Uncoupling of the first and second coupling elements results in minimal fluid contamination on the outer surfaces of the coupling elements. The bag connector systems provided herein are included in medical appliances for waste management.

Abstract: A composition for use on skin and wounds, comprising a photo-catalyst which is capable of preferentially staining biofilms the composition being for use in the diagnosis and treatment of biofilms in wounds.

Abstract: A stoma seal is described for a controlled evacuation ostomy appliance. The stoma seal may have a liquid-responsive property, such as hydrophobic, hydrophilic or absorptive. The stoma seal may have a non-smooth surface, e.g., at a microstructure scale. The non-smooth surface may consist of tortuous channels, protruding seals, or a confronting apertured or porous layer. The liquid-responsive property and/or the non-smooth surface may facilitate separation of flatus from faecal matter and/or facilitate venting of flatus while obstructing stool.

Abstract: The body has a fluid inlet port for receiving pressurized fluid and a fluid outlet port connected to the retention balloon. A first passage connects the fluid inlet port and the fluid outlet port. A second passage in the body is connected to the balloon fluid return path and is at the pressure of the retention balloon. A valve prevents fluid flow through the first passage when actuated. The valve includes a pressure-responsive member movable to a position to obstruct fluid flow in response to fluid pressure in the second passage exceeding the predetermined level. Flexible means such as a membrane defines a normally open portion of the first fluid passage, which is closed by the moveable means bearing on the membrane when pressure exceeding the predetermined level actuates the valve.

Abstract: Ostomy appliances with a filter system that is resistant to clogging by waste expelled by the stoma are provided for waste management.

Abstract: A stand-alone system for assessing wound exudates from the wound of a patient is described. The system contains functionality to detect, process and report various wound parameters. The system also may make treatment determinations based on these findings. The system may detect one or more physiological values of the wound exudates from the wound of the patient. The system may also compare detected physiological values to predetermined physiological values, in order to obtain a comparison result in real time. The system may include a processor (15) which provides an electronic signal based on the comparison result in which the electronic signal may corresponds to guidelines for treating the wound (3). The system described may be an accessory, which may be used on its own, or in conjunction with other wound treatment devices (9).

Abstract: A coupling assembly for fastening an adhesive wafer to an ostomy appliance device, the coupling assembly including a captive connection between the adhesive wafer and ostomy appliance that permits captive relative displacement between the entire adhesive wafer and the entrance aperture of the appliance, to facilitate access to the wafer from the non-body-contacting side. The coupling assembly further comprises a fixation coupling for fixing the adhesive wafer in the operative position.