Abstract: The invention provides an absorbent article comprising an indication means for indicating the presence of bodily exudates, the indication means comprising a color-changing indication means, wherein the absorbent article and the indication means form one integral unit, the article further comprising a indication device, which comprises a housing and a connection means, such that the indication device can be attached to the absorbent article and be detached from the absorbent article, wherein the indication device comprises a color sensor.

Abstract: A cerebral spinal fluid shunt plug includes a shunt plug housing having a recess formed therein and a shunt valve shaped and dimensioned for positioning within the recess of the shunt plug housing.

Abstract: Systems, methods, and apparatuses for treating a tissue site with reduced pressure are described. The system includes a manifold configured to be placed adjacent the tissue site, and a sealing member configured to be placed over the tissue site and the manifold. The system also includes a reduced-pressure source fluidly coupled to the manifold through the sealing member. The system further includes a pouch having an upstream layer having a first thickness, a downstream layer having a second thickness, and an absorbent member enclosed between the upstream layer and the downstream layer. The second thickness is greater than the first thickness. The upstream layer may have a hydrophilic side adjacent the absorbent member, and the downstream layer may have a hydrophobic side adjacent the absorbent member.

Abstract: Methods and apparatuses are disclosed relating to the creation and use of bespoke wound fillers and other wound treatment apparatuses. Some embodiments provide for the creation of bespoke wound fillers based on characteristics of a wound. Certain embodiments also include the use of bespoke wound fillers in combination with negative pressure to treat a wound.

Abstract: A topical applicator of the propel/repel type includes a reservoir, an attachable applicator cap, and a metered dosing system. The reservoir is suitable for mixing a topical formulation of multiple constituents using an electronic mortar and pestle and is closed using the applicator cap. Alternatively, the reservoir may be prefilled with a ready-to-use cream and medicament formulation, then sealed with a removable seal. The topical applicator can include a fast purge feature that overrides the metered dosing system to facilitate removal of air from the reservoir. The topical applicator can also include a one-way ratcheting feature to prevent reverse movement (repel) of the metered dosing system. Metered doses can be dispensed through holes in the applicator cap by rotating a knob, which has detent positions that correspond to discrete doses, and which provides audible and tactile feedback.

Abstract: A trap bottle assembly for mounting on a suction regulator or controller is disclosed. The trap bottle assembly includes a mounting adaptor for mounting on the suction regulator and a disposable trap bottle for releasable mounting on the mounting adaptor. The mounting adaptor includes a tubular connector and a body member having a peripheral sidewall from which a pair of pins extends. The threaded tubular connector connects the mounting adaptor to the suction regulator or controller. The trap bottle includes an annular flange for tightly engaging an undersurface of the body member to form a good fluid tight interface therebetween. The trap bottle includes a pair of recesses for receipt of the pair of pins, to enable the trap bottle to be releasably secured to the mounting adaptor.

Abstract: An apparatus and method for managing reduced pressure at a tissue site are disclosed. The apparatus comprises a pump for supplying reduced pressure to the tissue site, a motor coupled to the pump to propel the pump, and a drive system electrically coupled to the motor that includes a power source that provides a source of direct current power to the motor during an operational period at a substantially constant current and of sufficient magnitude to supply a targeted reduced pressure during the operational period. The drive system also includes a controller that monitors the pump's loading on the motor by measuring the voltage across the motor to determine whether the motor voltage remains within a predetermined operational range of voltages necessary for maintaining the reduced pressure supplied by the pump proximate to the targeted reduced pressure without directly measuring the reduced pressure using a pressure sensor.

Abstract: An ocular implant adapted to be disposed within Schlemm's canal of a human eye with a body extending along a curved longitudinal central axis in a curvature plane, a first strut on one side of the implant and a second strut on an opposite side of the implant, the circumferential extent of the first strut with respect to the plane of curvature being greater than the circumferential extent of the second strut with respect to the plane of curvature. The invention also includes methods of using the implant.

Abstract: An embodiment includes a wound dressing comprising: a shape memory polymer (SMP) foam, including open cells, having first and second states; and a hydrogel (HG) included within the cells; wherein (a) in a first position a composite, including the SMP foam and the HG, is configured to be located proximate a hemorrhagic tissue with the SMP foam in the first state; (b) in a second position the composite is configured to be expanded to the second state against the hemorrhagic tissue when the SMP foam is plasticized at 37° C. depressing a glass transition temperature (Tg) of the SMP foam to below 25° C. Other embodiments are described herein.

Abstract: The present invention relates to a suction device. The suction device comprises an attachment portion adapted to be attached to a wound cover member. The suction device comprises a fluid inlet which is at least partially circumscribed by the attachment portion. The suction device also comprises a fluid outlet. The suction device further comprising a connection portion adapted to, at least during one operation condition of the suction device, provide a fluid communication between the fluid inlet and the fluid outlet. The connection portion comprises an inspection portion that is transparent to thereby facilitate the positioning of the suction device relative to the wound cover member.

Abstract: An oxygenator unit adapted for use in an extracorporeal blood treatment device. The oxygenator unit includes an oxygenator having a gas inlet and a supply line for conducting a gas provided at the gas inlet, the supply line being connectable to a source of a pressurized gas containing oxygen, wherein the oxygenator unit further includes a pressure relief valve provided in the supply line upstream of the oxygenator, the pressure relief valve adapted to release pressure exceeding a predetermined pressure value from the supply line, thereby preventing a critical overpressure in the oxygenator.

Abstract: An applicator for a tampon comprising an inner tube slideable within an outer tube is provided. A plurality of protrusions is provided on the outer surface of the inner tube at its forward end and a plurality of spikes is provided on the inner surface of the outer tube at its forward end. The applicator has one or more of these features: i) the same or different number of protrusions and spikes; ii) one or more of the protrusions are arranged in an asymmetric manner around the outer surface of the inner tube such that the distance between two adjacent protrusions is not the same for all adjacent pairs of protrusions; iii) one or more of the spikes are arranged in an asymmetric manner around the inner surface of the outer tube such that the distance between two adjacent spikes is not the same for all adjacent pairs of spikes.

Abstract: A fill adapter for delivery of a medical liquid to a container has a body with a distal end, a proximal end, and a central bore extending between the distal end and the proximal end along a longitudinal axis. The central bore has an angled portion at the proximal end of the body such that a diameter of the central portion increases at the angled portion in a direction from the distal end to the proximal end. The fill adapter further has a flow controller disposed within the central bore at a distal end of the angled portion such that a gap is formed between an outer surface of the flow controller and an inner surface of the central bore. The flow controller is shaped to direct liquid flowing through the central bore to flow through the gap and along the angled portion of the central bore under a Coand? effect.

Abstract: The disclosure relates to a wound dressing comprising a fibre fleece-based body, and a packaging forming the outer visible sides of the wound dressing, which packaging contains a layer made from a flat textile on the side of the wound dressing facing the wound, which has an outer-side, partially and structurally applied coating, and wherein the packaging has a fibre fleece layer on the side of the wound dressing facing away from the wound, which forms the outer visible side of the wound dressing; and, a liquid-impermeable plastic film layer on the side of the fibre fleece layer facing the wound, and wherein the fibre fleece layer, the plastic film layer, the body and the textile layer are not connected to one another, but rather lie with the flat sides thereof loosely and movably against one another and are only connected along the peripheral edges by a joint connection.

Abstract: A nozzle and an ear cleaning device are disclosed. The nozzle includes: a main body, where the main body is provided with a first hole portion penetrating in a front-rear direction; and a housing, where the housing is connected to the main body and surrounding a periphery of the main body, the housing is provided with a guide portion and a plurality of drainage portions, the guide portion has an outer diameter gradually increasing from a front end of the main body to a rear end of the main body, the plurality of drainage portions are arranged at intervals in a circumferential direction of the housing, and each of the drainage portions is communicated with the front end of the main body and extends from the front end of the main body toward the rear end of the main body.

Abstract: Device for packaging and dispensing drops of a substance for ophthalmic use, generally fluid, semi-fluid or in suspension, emulsion or oily solution including a dispensing accessory with a first valve made of an elastomer material that allows the substance to pass through when the dispensing accessory is stressed, without allowing outside air to pass through in the opposite direction when the dispensing accessory is relaxed, characterized in that the first valve is covered by a layer of Parylene.

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.

Abstract: Systems, apparatuses, and methods for instilling fluid to a tissue site in a negative-pressure therapy environment are described. Illustrative embodiments may include a pneumatically-actuated instillation pump that can draw a solution from a solution source during a negative-pressure interval, and instill the solution to a dressing during a venting interval. A pneumatic actuator may be mechanically coupled to a disposable distribution system that can provide a fluid path between the solution source and a distribution component. A bacterial filter may be disposed in the fluid path between the actuator and the distribution component to prevent contamination of the actuator during operation. The distribution system may be separated from the actuator and disposed of after operation, and the actuator may be re-used.

Abstract: A packaged closed intermittent urinary catheter system equipped with a dispensing system and method of dispensing a packaged catheter using the dispensing system. The dispensing system is a pair of separately translatable movement control devices, each operably engaging the catheter for permitting unidirectional movement of the catheter in a first axial direction relative to the movement control devices. The movement control devices may be mounted to a hand-grippable assembly with a sliding or pivoting movable member reciprocal to a base member. Alternatively, the movement control devices are mounted to a coupling member and a spring member biases them apart.

Abstract: Devices can be implanted in an eye to treat a dry eye condition. The devices include a body defining a lumen and having first and second ends and external and lumenal surfaces. The body has a length sufficient to provide fluid communication between the anterior chamber and tear film of the eye through the lumen when the device is implanted in the sclera. In some embodiments, the device is filterless. In some embodiments, a filter is included. The dry eye treatment devices provided herein prevent bacterial ingress, provide outflow resistance to retain a normal intraocular pressure, and provide moisture (e.g., aqueous humor) to an otherwise dry eye. Methods of treating a dry eye condition wherein the device is implanted in the sclera of an afflicted eye are also described.