Abstract: The present disclosure provides a method performed in an accessory device. The accessory device comprises an interface configured to communicate with one or more devices of an ostomy system. The interface comprises a display. The ostomy system comprises a monitor device, and/or an ostomy appliance configured to be placed on a skin surface of a user, wherein the ostomy appliance comprises the base plate. The method comprises displaying, on the display, a notification settings user interface comprising one or more control objects including a first control object, wherein the notification settings user interface is configured to adjust notification setting parameters of an ostomy user application.

Abstract: An ostomy device includes a nonwoven element having a water-soluble component and a releasable material. When the ostomy device is applied to a user and stomal output contacts the distal surface of the nonwoven element, the water-soluble component dissolves and releases the releasable material from the nonwoven element to neutralize at least one of enzyme activity and pH of the stomal output.

Abstract: According to some embodiments of the invention, an anchoring system includes a sleeve having an inner surface defining a first lumen, a first annular sealing mechanism disposed at a proximal end of the sleeve, and a second annular sealing mechanism disposed at a distal end of the sleeve. The anchoring system further includes a pressure tube in fluid connection with an outer surface of the sleeve, a sheath in mechanical connection with the sleeve, the sheath forming a second lumen, the second lumen being in fluid connection with the first lumen, and open-cell foam disposed on the outer surface of the sleeve. Application of negative pressure to the pressure tube causes a seal to form between the first and second annular sealing mechanisms and an inner surface of a tissue cavity. Application of negative pressure to the pressure tube also creates a frictional force that resists displacement of the sleeve.

Abstract: An asymmetric multilayer film for an ostomy pouch includes a barrier layer including a first side and a second side. At least one layer is arranged on the first side of the barrier layer, and at least one layer arranged on the second side of the barrier layer, in which the combined thickness of the at least one layer arranged on the first side of the barrier layer is at least two times greater than the combined thickness of the at least one layer arranged on the second side of the barrier layer. The asymmetric multilayer film has a thickness of about 25 ?m to about 50 ?m.

Abstract: A drainage bag system for urinary collection includes a urinary drainage bag having a first inlet and an inlet valve for regulating a flow of urine from a catheter into the urinary drainage bag via the first inlet, an outlet, and an outlet valve for regulating a flow of urine out of the urinary drainage bag. The drainage bag system further includes a receptacle bag of a foil or sheet material for emptying the urinary drainage bag and having a receptacle compartment for storing urine and a connector for providing a connection between the receptacle bag and the urinary drainage bag. The connector provides a second inlet constituting a receptacle inlet to the receptacle compartment when connected to the receptacle bag such that urine can flow into the receptacle compartment.

Abstract: A method of detecting ostomy effluent leakage in an ostomy appliance is provided. The method includes the steps of providing a plurality of sensors; measuring resistance of the ostomy appliance using each of the plurality of sensors; entering resistance measurements in a ring buffer configured to hold resistance measurements; calculating a median resistance value of each of the plurality of sensors using the resistance measurements; comparing the median resistance value against a predetermined range of acceptable resistance values; increasing a leak count for a corresponding sensor when the median resistance value of the sensor is outside the predetermined range of acceptable resistance values; determining a leak state when the leak count increases beyond a predetermined acceptable leak count; and sending an alert upon a determination of a leak state.

Abstract: In an example, a urine collection device includes a covering defining a recessed receptacle and a fluid collection assembly positioned in the recessed receptacle. The fluid collection assembly includes (i) a foam sleeve including a bore, (ii) a shape retaining element positioned in the bore of the foam sleeve and defining a passage, and (iii) a tube extending through the passage defined by the shape retaining element. The shape retaining element can conform the fluid collection assembly to a curved configuration and maintain the curved configuration of the fluid collection assembly until the curved configuration is adjusted. The urine collection further includes a top sheet coupled to the covering. The top sheet and the covering define an internal chamber of the urine collection device. The top sheet is configured to draw urine into the internal chamber and toward the fluid collection assembly.

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

Abstract: An ostomy appliance having an appliance wall of flexible sheet material forming a cavity for containing a stomal output. The wall has a stomal inlet for receiving the stomal output and a gas vent for allowing the stomal gas to migrate out of the cavity. A filter arrangement is mounted to the appliance wall and has a filter channel extending from a filter channel inlet to a filter channel outlet. The filter channel inlet is located in the cavity for receiving the stomal output from the cavity and the filter channel outlet is mounted in communication with the gas vent for allowing stomal gas to migrate out of the filter channel to the gas vent. A separation element extends along the filter channel for maintaining the filter channel in an open configuration along part of the filter channel for allowing stomal gas to pass therethough.

Abstract: A menstrual device with a reservoir portion attached to a rim portion where the rim of the device is configured to improve use and comfort. The edge of the reservoir portion may be molded into the defined geometry of the rim portions. Additionally, the rim may have one or more channels and/or elements positioned within the defined geometry of the rim.

Abstract: Systems and methods for component stress relief are disclosed. In some embodiments, a wound dressing includes a substantially stretchable wound contact layer including a wound facing side and a non-wound facing side. The wound facing side or the non-wound facing side of the wound contact layer can support a plurality of electronic components and a plurality of electronic connections that connect at least some of the plurality of the electronic components. The wound facing side or the non-wound facing side of the wound contact layer can include a region of substantially non-stretchable material that supports at least one electronic component from the plurality of electronic components. The at least one electronic component can be attached to the wound contact layer with adhesive material. Such arrangement can securely position the at least one electronic component and limit the mechanical strain on the at least one electronic component supported by the region.

Abstract: Provided is a ureteral stent comprising certain amount of ethylene-vinyl acetate polymer and a certain amount of an additive selected from barium sulfate, bismuth subcarbonate, bismuth oxychloride, a polyolefin elastomer, a thermoplastics elastomer, and a mixture thereof. The provided stent may have multiple layers such as inner layer and outer layer with each layer having different elastic modulus. Also provided is a method of making the aforementioned ureteral stent and a method of using the ureteral stent in treating kidney or bladder related diseases.

Abstract: Various systems, devices, and methods for endovascular implants and placement thereof are disclosed. The implants include a proximal implant segment, a distal implant segment, connector struts connecting the proximal implant segment to the distal implant segment, and a side opening between the proximal implant segment and the distal implant segment. The implants can be used to create an arteriovenous fistula or connect one vessel of the body to another by placement of the proximal implant segment and the distal implant segment within the vessels to be connected. The implants can include one or more anchors for securing the implant in place with respect to the vessels of the body it is connecting. The implants can also include a continuous strut or ring at a distal edge of the proximal implant segment. Also disclosed are methods for percutaneous placement of the implants, and a device for percutaneous delivery.

Abstract: A monitor device for an ostomy system comprising an ostomy appliance with a base plate and a method of monitoring an ostomy appliance is disclosed.

Abstract: A monitor device for an ostomy system is disclosed. The monitor device comprises a first interface comprising a primary terminal and a secondary terminal. The primary terminal is configured to form electrical connection with a primary electrode of the base plate when the monitor device is coupled to the base plate, and the primary terminal being configured to form electrical connection with a primary charge terminal of the accessory device when the monitor device is coupled to the accessory device. The secondary terminal is configured to form electrical connection with a secondary electrode of the base plate when the monitor device is coupled to the base plate, and the secondary terminal being configured to form electrical connection with a secondary charge terminal of the accessory device when the monitor device is coupled to the accessory device.

Abstract: Assembly with connectable and disconnectable elements comprises a flexible bag containing liquid solution with a first valve connector, at least one vial with active substance and provided with a hermetic closing cap, a coupling and piercing device couplable to the cap of the vial and an adapter between the first connector and the coupling and piercing device. The adapter has a hollow external body with a first end fixable by screwing to the first connector, an axially bored, coaxial internal stem, the screwing causes the opening of the first connector and a second end including a second valve connector fixable to the coupling and piercing device and is screwable in the external body so that internal stem causes the opening of the second valve connector.

Abstract: Examples relate to fluid collection devices, systems, and methods of collecting fluid from wearers. The fluid collection devices include a retention means for maintaining the position of the fluid collection device with respect to the wearer.

Abstract: A reusable menstrual discharge collection device is described comprising: dual durometer article that forms a menstrual discharge disc-shaped collection device with a half spherical dome catch where the half spherical dome catch includes a continuous circumferential top and bottom portion, and wherein the continuous top portion is attached to a continuous uniform flexible hinge that is placed along an entire circumferential uniform upper portion of the half spherical dome catch and wherein the hinge also forms a base for and is connected to a 360-degree continuous uniform circumferential rim section such that the hinge allows the half spherical dome catch to be in both an inverted use position/configuration that allows movement of the catch toward the rim section allowing for adjustability to fit multiple cervix physiologies and the elongated configuration allows for ease of manufacturing and cleaning.

Abstract: A reduced-pressure system for treating a tissue site on a patient includes a distribution manifold that adheres to a tissue site to allow retention without external support. The distribution manifold includes a porous member and a tissue-fixation element. The tissue-fixation element maintains the porous member substantially adjacent to the tissue site while a sealing member is applied. In one instance, the tissue-fixation element is a soluble adhesive that partially covers either the tissue-facing side of the porous member or a tissue-facing side of a fluid-permeable substrate layer that is on the tissue-facing side of the porous member. Other systems, distributions manifolds, and methods are presented.

Abstract: A medical device includes a monitor having a processor for processing data and a memory adapted to store the data, and a medical appliance attachable to skin of a user. The medical appliance includes an adhesive, an electrode assembly coupled to the medical appliance and located distal to the adhesive, a top layer coupled to the medical appliance and located distal to the electrode assembly, and a monitor interface connected to the top layer. The monitor interface includes a mechanical coupling part to mechanically attach the monitor to the medical appliance and an electrical coupling part with a terminal that electrically connects the monitor to the electrode assembly when the monitor is attached to the medical appliance.