Abstract: An ostomy barrier extender includes a skin friendly adhesive layer, a backing layer laminated on a surface of the skin friendly adhesive layer, a release liner laminated on an opposite surface of the skin friendly adhesive layer, at least one perforated feature, an outer periphery, an inner periphery, and a ring shaped body defined between the outer periphery and the inner periphery. The ostomy barrier extender is configured to separate along at least one perforated feature.

Abstract: Glaucoma treatment devices are disclosed. In various example, the glaucoma treatment devices include a body and a fluid conduit that are configured to help facilitate evacuation of fluid from a fluid-filled body cavity, and reabsorption of the evacuated aqueous humor by the body through tissue surrounding the glaucoma treatment device. In some examples, the glaucoma treatment device is configured such that a flow resistance through the fluid conduit can be modified post-operatively one or more times.

Abstract: A piercing part for a medical infusion system includes a housing with a piercing mandrel, a fluid channel and a ventilation channel with a first channel portion extending at least substantially parallel to the fluid channel and with a second channel portion diverted towards an outside of the housing and to which an air filter element and a fluid shut-off member are assigned. A drip chamber can include a piercing part. The piercing part can be produced by an injection molding tool. The second channel portion in the housing is oriented parallel to the first channel portion and open towards an inside of the housing. An open region of the channel portion is closed by a separately produced closure part. The piercing part can be used with a medical infusion system.

Abstract: An insertion end for a tampon applicator assembly. The insertion end has an insertion tip region and optionally an inflection region. The insertion end of the tampon applicator assembly is unique in one or more ways, including one or more of the following: having a unique degree of closure, an inflection region length that is different than an insertion end region length, petal slits that form a tear-drop shape, petals having multiple radii of curvature, the insertion end having a unique radius of curvature, the insertion end having a unique part thickness.

Abstract: An embodiment of a uterine hemorrhage controlling system comprises a suction module including a suction end coupleable to a pump by a connecting tube, and a sealing module coupled to the suction module. The system may further comprise the pump and a filter coupled to the suction module. A uterine hemorrhage controlling method comprises: shielding a suction module that has been delivered into a uterus; sealing an entrance into the uterus while the suction module is situated within the uterus; applying a negative pressure within the uterus upon activation of a pump; and maintaining the negative pressure within the uterus to induce uterine contraction. The method may further comprise delivering the suction module into the uterus; transmitting bodily fluids, out of the uterus through the suction module, and filtering the bodily fluids.

Abstract: A surgical device, system and method for forming opening in the trabecular meshwork of eyes to facilitate drainage of aqueous humor and resultant lowering of intraocular pressure are provided. The device comprises a shaft and a distal member or foot on a distal end of the shaft. The distal member or foot may have a forward tip, a right edge, a left edge and a transversely concave depression, cavity or space between the right and left edges. The distal member is insertable into Schlemm's canal of an eye and thereafter advanceable through Schlemm's canal such that trabecular meshwork tissue will be cut by the right and left edges.

Abstract: An embodiment of a uterine hemorrhage controlling system comprises a suction module including a suction end coupleable to a pump by a connecting tube, and a sealing module coupled to the suction module. The system may further comprise the pump and a filter coupled to the suction module. A uterine hemorrhage controlling method comprises: shielding a suction module that has been delivered into a uterus; sealing an entrance into the uterus while the suction module is situated within the uterus; applying a negative pressure within the uterus upon activation of a pump; and maintaining the negative pressure within the uterus to induce uterine contraction. The method may further comprise delivering the suction module into the uterus; transmitting bodily fluids, out of the uterus through the suction module, and filtering the bodily fluids.

Abstract: A method for altering the appearance of molded articles is described herein. The method includes the steps of providing a plurality of articles; feeding a first article to a conveyor; transporting the first article to a treatment station; activating an activatable colorant of the first article by exposing the first article to at least one energy source, thereby causing a color change in the first article; manipulating the exposure of the first article to create a first discernable pattern in the first article; feeding a second article to the conveyor; transporting the second article to the treatment station; activating an activatable colorant of the second article by exposing the second article to the at least one energy source, thereby causing a color change in the second article; and manipulating the exposure of the second article to create a second discernable pattern in the second article.

Abstract: The purpose of the invention is to create a urine bag that can be easily folded in order to occupy less space prior to use and that can be easily manipulated by a patient, in particular a paraplegic patient. This is achieved using a urine collection bag (1) formed by two sheets of plastic material that are stacked and welded along the periphery (2) thereof. The collection bag (1) comprises a collection compartment (3), said inlet being in communication with the intake port (4) and delimiting the upper portion of the collection compartment (3). The intake port (4) is provided with a vertical extension (8) closed along their periphery (22) thereof and comprising a urinary catheter (9). The bag (1) of the invention is characterised in that the intake port (4) and the inlet (6) are offset vertically, and in that the vertical height (ho) of the bag (1) corresponds to a multiple of the height (hp) of the extension (8).

Abstract: Disclosed is an ostomy device with an adhesive wafer for attachment to a skin surface of a user and a collecting bag for collecting output from a stoma. The collecting bag is connected to the adhesive wafer, and the adhesive wafer has a through-going hole for accommodating the stoma of the user. The adhesive wafer includes a backing layer, a first switchable adhesive composition, a second adhesive composition, and a release liner. The first adhesive is contained in a recess in the device. The first switchable adhesive composition comprises a polymer and a switch initiator, and can be switched from a first liquid state to a second adhesive state by activation of the switch initiator.

Abstract: The present invention provides a tampon pledget with one or more of the following properties: increased absorbency rate; high absorbent capacity and fluid retention; rapid expansion potential; and ease of ejection of the pledget from the applicator. Surprisingly, the one or more properties are achieved by using a modified dual cross-pad, folded, compressed tampon pledget design.

Abstract: A system or apparatus may include a container configured to collect fluid from a tissue site and regulate negative-pressure from a negative-pressure source. In some embodiments, the container may include a regulator that receives negative pressure directly from an unregulated negative-pressure source, such as a wall-suction outlet. The regulator may regulate down the pressure delivered to a collection chamber in the container, which may in turn be connected to a tissue site.

Abstract: A non-invasive female urine collection device comprising a first pipe with an inflatable balloon attached to a first end of the first pipe; and a urine collection member attached to a second end of the first pipe such that, when the first end of the first pipe is inserted into vagina, the urine collection member covers urethra for collecting the urine discharged through the urethra. The urine collection member further comprising a first membrane and a second membrane together forming a urine collection pouch, in that the second membrane is shorter than the first membrane exposing the first membrane around Urethra for collecting the urine discharged through the urethra. The urine collection member further comprising a set of spikes formed on the first membrane in line with the urethra to prevent splashing of urine coming out of urethra.

Abstract: An ostomy bag can include one or more sensors for measuring one or more metrics. An ostomy wafer can also include one or more sensors for measuring one or more metrics. The sensors can be temperature sensors and/or capacitive sensors, for example, and the metrics can include bag fill, leakage, skin irritation, and phase of stoma output, among others.

Abstract: Described herein is a child-resistant topical drug applicator and methods of applying a topical pharmaceutical composition to a surface. In one aspect, the child-resistant topical drug applicator comprises a container comprising a connector and a tube configured to contain a topical pharmaceutical composition, a sponge applicator fluidly coupled to the connector, and a child-resistant cap that reversibly couples to the connector and encloses the sponge applicator, the cap having a locked position and an unlocked position. Also described herein are methods of opening and using the child-resistant topical drug applicator.

Abstract: An eye drop guide includes a frame including at least one eye-covering member, and a plurality of apertures arranged in columns, each column having multiple apertures, the apertures in each column being vertically offset from apertures in adjacent columns.

Abstract: The present disclosure relates to methods for sealing absorbent cores of disposable diaper pants during the assembly process. The diaper pants may include a chassis connected with a ring-like elastic belt. Aspects of the assembly methods involve bonding a continuous length of absorbent cores between a continuous topsheet substrate and a continuous backsheet substrate advancing in a machine direction. The combined continuous topsheet substrate, continuous backsheet substrate, and continuous length of absorbent cores are then cut along a cross direction to create discrete chassis, wherein the topsheet, the backsheet, and the absorbent core of each chassis have equal longitudinal lengths. The discrete chassis are then deposited onto a first continuous elastic laminate and a second continuous elastic laminate. Opposing end regions of the absorbent cores may then be sealed by positioning a sealing layer across the topsheets of the chassis.

Abstract: An implantable actuation device that may be used with a glaucoma drainage device or attached to an ocular surface, a method of making an implantable actuation device, and a method of preventing cell adhesion resulting from a glaucoma treatment procedure. The implantable actuation device is made from a magnetoelastic material. Actuation of the magnetoelastic material may help control cellular adhesion that may develop and undesirably disrupt proper healing when recovering from invasive surgical treatments. The implantable actuation devices may have small form factors and customized geometries which include three-dimensional curvatures to help promote the actuation of liquid flow and facilitate the removal of unwanted cells.

Abstract: Embodiments described herein generally relate to improved devices, systems, kits, products and methods related to topical medicament application of measured dosages. The kits and devices can single use and/or disposable for example.

Abstract: An absorbent garment has a minimum crotch width less than 30% the front region width. The absorbent garment has an absorbent member minimum width less than 80 mm. The absorbent member minimum width is less than 53% the minimum crotch width and is less than 60% the absorbent member maximum width.