Abstract: A defecation detection device (2) is adapted to communicate with a receiver (4) and includes a mounting seat (21), a resilient member (22) having a fixed end (221) that is connected to the mounting seat (21) and a free end (222) that is spaced apart from the mounting seat (21), a first conductive sheet (51) that is disposed on the free end (222) of the resilient member (22), a second conductive sheet (52) that is disposed on the mounting surface (211) of the mounting seat (21), and a transmitter module (6). When the free end (222) of the resilient member (22) is pressed to move toward the mounting seat (21), the first conductive sheet (51) is in contact with the second conductive sheet (52), and the transmitter module (6) is configured to wirelessly transmit a signal to the receiver (4) to allow the receiver (4) to output a notification.

Abstract: Provided is a bandage composition dispenser and/or applicator that includes a nozzle and a cap. In some embodiments, the dispenser and/or applicator is used to dispense a bandage or dressing composition that forms a durable film bandage or skin protectant.

Abstract: A manifold for collecting a tissue sample with a medical waste collection assembly. A base portion of a housing is removably engaged with a manifold receiver to provide a suction path from an inlet fitting receiving a suction line. A tray may be removably positioned within an accessory sleeve. Locating features facilitate defining a gap between a base portion of the tray and a lower barrier of the accessory sleeve. The tray may include a control surface to move the manifold between a sealing configuration, and a bleed configuration in which a second suction path is provided through the gap and below the tray. A backflow prevention valve may be disposed within the suction path between the tray and a filter element. Methods for collecting the tissue sample are also disclosed.

Abstract: An integrated catheter assembly includes a housing member, an outer lumen member extending from the housing member, and a needle member slidably or movably coupled to the housing member, wherein the needle member can be extended beyond a first port of the outer lumen member in a first position and concealed in the outer lumen member in a second position. The outer lumen member has a side port between its first and second ports such that when the needle is extended in the first position and inserted into an arteriovenous fistula, blood from the arteriovenous fistula flashes into the needle member, is diverted through a relief port of the needle member out the side port of the outer lumen member for delivery to a dialysis machine. The assembly further includes an inner lumen member that is disposable through the housing member to extend out from the same the outer lumen member to provide dialyzed blood from the machine. The assembly therefore receives and delivers blood through a single injection site.

Abstract: An extension assembly for a catheter comprises an extension tube, an extension connector, and an indicator assembly. The extension tube has a proximal end and a distal end. The extension tube further has an inner bore and an opening placing an interior of the extension tube in fluid communication with an exterior of the extension tube. The extension connector is coupled to the proximal end of the extension tube. The indicator assembly is comprised of a sealing member, a wicking member, and an indicator. The sealing member including a first side and a second side. The wicking member includes a wicking tab to be disposed within the opening of the extension tube. The indicator is in fluid communication with the wicking member. The sealing member is at least partially clear to allow visual inspection of the indicator once the indicator assembly is coupled to the extension tube.

Abstract: An extension assembly for a catheter having an extension tube, an extension connector and an indicator assembly. The extension tube has a proximal end and a distal end, and, an inner bore. The extension connector has a body with a central bore, with the proximal end of the extension tube coupled to a first end of the body. The extension connector further includes a slot in the body defined by lower end wall and upstanding walls extending therefrom, terminating at an upper opening. A radial passage extends from the central bore to the at least one slot. The indicator assembly has an indicator that is structurally configured to change color in the presence of a chemical indicative of a bladder infection. A wicking member is in fluid communication with the radial passage and the indicator, with the wicking member being positioned between the radial passage and the indicator.

Abstract: An ocular implant is constructed of a clear, transparent, biologically compatible material and includes a hydrophilic outer surface configured for continuous attachment to a posterior surface of a cornea. The ocular implant has a first radius of curvature at initial attachment to the posterior surface of the cornea and a second radius of curvature at post-initial attachment to the posterior surface of the cornea. The first radius of curvature is different than the second radius of curvature. The ocular implant remains attached to the posterior surface of the cornea at both the first and second radii of curvature.

Abstract: A dermal adhesive patch is provided. The dermal adhesive patch is adhered to skin through an ampoule containing a mixing ingredient, a drying ingredient, a viscosity control ingredient, and a moisturizing ingredient. The dermal adhesive patch includes: a support body; and a membrane layer formed as a nanofiber web having pores to block moisture and to allow air to pass through the membrane layer, and detachably laminated on one surface of the support body.

Abstract: A device for containing waste material leaking from the junction between a stoma and a stoma bag having a flange, the device comprising a flange extension member which circumferentially surrounds the stoma bag flange and wherein the flange extension member includes a pouch for holding a spare stoma bag. The flange extension member can comprise an absorbent layer and can be sealed to the user's skin at its outer edge. Additionally, the flange extension member can have a waterproof or impermeable backing layer to prevent waste material from seeping through it. The device can be included in a modified stoma bag flange and a modified stoma bag.

Abstract: An aspiration system to control vacuum pressure in an ultrasonic surgical handpiece to result in improved control responsiveness during aspiration. The system comprises a console including a vacuum pump. The system includes a cassette comprising a joint that divides a vacuum path into at least two flow paths. A first joint port couples to a first flow path. A second flow path is coupled to a second joint port, a third flow path is coupled to a third joint port, and a fourth flow path is coupled to a port on a surgical waste receiver. A first sensor senses pressure in the fourth flow path and provides a waste receiver pressure signal. A second sensor senses pressure in the third flow path and provides a tip pressure signal. The controller controls a position of a first vent valve and a second vent valve based on the waste receiver pressure signal and the tip pressure signal, respectively.

Abstract: A method for manufacturing an inner drainage biomimetic stent for glaucoma. The inner drainage biomimetic stent for glaucoma comprises: a cylinder tube body with a hollow structure, and a plurality of straight tubes, provided inside the hollow structure of the tube body, for supporting a tube wall of the tube body. Proper placement of the inner drainage biomimetic stent for glaucoma can direct an aqueous humour to smoothly flow through an orifice expanded by the biomimetic stent, into Schlemm's canal.

Abstract: A disposable absorbent article. The disposable absorbent article has a topsheet; a backsheet; and an absorbent core disposed between the topsheet and the backsheet. The disposable absorbent article exhibits a pad peel force of at least about 0.5 N, when measured in accordance with the product integrity test.

Abstract: A method of inducing retrograde blood flow may include extending a sheath through opposite walls of one of an artery and a vein of a subject and through a wall of the other of the artery and the vein such that a distal end of the sheath may be positioned within one of the artery and the vein. The method may include inducing retrograde blood flow in the artery and delivering the induced retrograde blood flow into the vein of the subject via the sheath.

Abstract: A smoke evacuator for use with a surgical access device includes an evacuation ring having an inner peripheral surface defining one or more channels therein disposed in fluid communication with an operating cavity. A connection port is disposed thereon in fluid communication with the channel(s) and adapted to connect to a smoke evacuation system. The evacuation ring includes a profile having an inner flange that forms part of the inner peripheral surface of the evacuation ring and one or more lower flanges, the inner flange is configured to mechanically engage a rim of an access device and the lower flange(s) is adapted to mechanically engage a wound guard, wherein engagement of the inner flange of the evacuation ring atop the access device and engagement of the lower flange(s) with the wound guard secures the access device, the wound guard and the smoke evacuation ring within the operating cavity.

Abstract: A gastrointestinal device and methods of use thereof for the treatment of metabolic disorders is provided. The gastrointestinal device features disintegrable sleeve configured to fit within a patient's duodenum and to carry fluid (e.g., liquid or semisolid material, for example, chyme and digestive secretions) from its proximal end to its distal end.

Abstract: A urine collection device for collecting a sterile urine sample. The urine collection device may include a seat portion supported by a seat base. The portion includes a backrest and a saddle that projects from the seat portion. The saddle has an opening to a collection element that includes a cup mount to locate a urine collection cup within the collection element.

Abstract: A stent including a tubular body formed of one or more interwoven wires, a first anchor member disposed adjacent the first open end of the stent, a second anchor member disposed adjacent the second open end of the stent, and at least one divider disposed between the first and second anchor members. The first and second anchor members and the divider extend radially outward from the tubular body to divide the tubular body into at least a first saddle region extending between the first anchor member and the divider and a second saddle region extending between the second anchor member and the divider.

Abstract: An external female urinary device includes a connecting and urine collecting component (CUCC) and a urine directing and discharging component (UDCC) configured to connect with the CUCC. The CUCC tapers from a larger orifice to a smaller orifice. The CUCC has a ring defining the larger orifice. The ring is made of a material capable of adhering to urethral orifice surrounding skin (UOSS) as well as to the inner facing surfaces of the labia minora and/or the labia majora after the CUCC is pressed against that UOSS. The ring remains adhered to the UOSS without requiring an external force for keeping the ring in contact with that skin.

Abstract: Fecal management methods and apparatuses (e.g., devices, systems, etc.) may apply one or more fecal removal cycles of suction and irrigation (and in some examples air) to actively remove fecal material. The apparatus may control the timing of delivery of the fecal removal cycles as well as the parameters of the applied suction, irrigation and/or air within and between fecal removal cycles.

Abstract: An absorbent article includes a liquid permeable top sheet, a liquid impermeable back sheet, and an absorber provided between the two sheets, the absorbent article having a predetermined length in a front-to-rear direction, and a predetermined width in a width direction perpendicular to the front-to-rear direction, wherein the absorber is provided with a groove or a slit extending in the front-to-rear direction, the absorber includes a first absorber layer on the side closer to the top sheet, and a second absorber layer on the side closer to the back sheet, and the first absorber layer includes a high-stiffness part extending outward in the width direction from an edge portion of the groove or slit, and a stiffness of the high-stiffness part is higher than a stiffness of the second absorber layer.