Abstract: A formed film includes a first surface generally located in a first plane, a second surface generally located in a second plane parallel to and spaced from the first plane, and a third surface generally located in a third plane parallel to and spaced from the first plane and the second plane, in between the first plane and the second plane. A porous structure extends between the second surface and the third surface. A plurality of raised areas have sidewalls that extend between the first surface and the third surface, and top portions that define the first surface. The plurality of sidewalls, the porous structure, and the first plane define a plurality of gathering volumes.

Abstract: A urinary catheter assembly having a sleeve is provided. The urinary catheter assembly comprises a urinary catheter (2) having a hydrophilic surface; the urinary catheter being provided with an insertion tip (5) in a proximal insertion end of the urinary catheter and an outlet (4) at a distal end of the urinary catheter, a handle (8) being slidingly disposed on the urinary catheter, a collapsible, flexible sleeve (7) attached to the handle and being configured to cover the urinary catheter from the outlet to the tip portion in an extended configuration of the urinary catheter assembly, the sleeve being attached to a connector (9) at the outlet, the connector and handle configured to be detachably attached to each other and define a cavity provided by the sleeve, handle and connector encapsulating an entirety of the urinary catheter in a storage condition.

Abstract: A retention cuff is disclosed for retaining a fluid collection device or system in an orifice of a patient. The retention cuff has a body has a central opening and an inflationless cuff wall that includes an annular cuff wall and one or more side elements. The retention cuff is non-inflatable and has a self-deployed state or shape. The retention cuff can be coupled to a fecal collection device such that the central opening is in flow communication with a collection tube of the device and with the body of the retention device.

Abstract: A sterile dual-purpose closed intermittent urinary catheter system that may be used as either a drain line or a collection bag. A catheter resides within an inner cavity of an extensible sheath and may be extracted from a forward end through an outlet hub for insertion into the urethra. A valve at a rearward end of the sheath may be opened to permit the sheath to function as a drain line, or closed to permit the sheath to function as a collection bag. The sheath has an extended length substantially longer than the catheter length, and may be compressed in an accordion fashion or folded to a compact packaged shape. The urine may be collected in the sheath with the valve closed, or drained straight into a toilet with the valve open. The system may have a source of lubrication to wet the catheter.

Abstract: The present invention provides a device and method for preventing or curing pressure ulcers or chronic wounds. A multilayer dressing comprises a soft silicone jell layer of a suitable thickness which is placed in the multilayer dressing, above an absorbent layer. The matrix of the silicone jell layer is populated with a plurality of silicone beads of suitable size. The beads are connected to each other, and to the silicone jell layer. Breathing of wound and substantial supply of oxygen to the wound is duly insured for all layers of the multiple layer dressing. The beads play a pivotal role in promoting the effectiveness and performance of the multilayer dressing by acting as the plurality of effective cushions, as they absorb and uniformly redistribute a patient's body weight across the entire applied dressing area. The low adhering adhesive coating of about 5 mm in width is applied to the peripheral edges of all the layers.

Abstract: Systems and methods for controlling a pump system for use in negative pressure wound therapy are described herein. In some embodiments, a method for controlling a pump system includes applying a drive signal to a pump assembly of the pump system, the drive signal alternating between a positive amplitude and a negative amplitude and the drive signal having an offset, and sampling a pressure within a fluid flow path configured to connect the pump system to a wound dressing configured to be placed over a wound during one or more time intervals. Each of the one or more time intervals can occur when the drive signal is approximately at an amplitude equal to one or more sampling amplitudes.

Abstract: A blood coagulant assembly having a blood coagulant device adapted to be placed into a nostril of a patient suffering from a nose bleed. The blood coagulant device being initially placed within a blood coagulant device container which has a top section and a bottom section each secured to the other in a releasable manner. The blood coagulant device being mounted in a fixed position within the blood coagulant device container prior to removal of the blood coagulant device for insertion into a patient's nose that is bleeding. The blood coagulant device having a handle lower section and a handle upper section with a through opening passing through both the lower and upper handle sections. A blood coagulant material is secured onto an outer surface of the blood coagulant device to be placed against an inner surface of the nostril of a patient that is experiencing a bleeding nose for the purpose of stopping the nose from bleeding.

Abstract: Disclosed is a device for separating a cellular component from a multicomponent fluid. The device can include a body, a first acoustic wave generator, and a second acoustic wave propagating component. The body can define a channel having a first surface, an opposing second surface, a first side, and an opposing second side. The channel can extend along a longitudinal axis from a first end to an opposing second end. The first acoustic wave generator can be coupled to the first surface. The second acoustic wave propagating component can be coupled to the second surface. The first acoustic wave generator and second acoustic wave propagating component can be configured to generate a bulk standing acoustic wave in the channel.

Abstract: A medical fluid management assembly includes: a pneumatic manifold including a plurality of pneumatic passageways and a plurality of pneumatic connectors; a pump and valve engine including a plurality of valve chambers and at least one pump chamber, the pump and valve engine including a plurality of pneumatic connectors mated sealingly and releaseably with the pneumatic connectors of the pneumatic manifold, the pump and valve engine further including a plurality of fluid connectors; and a fluid manifold including a plurality of fluid pathways and a plurality of fluid connectors mated sealingly and releaseably with the fluid connectors of the pump and valve engine.

Abstract: An apparatus and use thereof for clearing a capsular space following removal of a cataract or other ophthalmologic procedure. The apparatus includes a body having an irrigation outlet, an aspiration inlet, and a sweeper head rotatably connected with the body for extending a portion of the body including the irrigation outlet, the aspiration inlet, and the sweeper head into the capsular space. The sweeper head is connected with the body by a flow-to-rotary converter located in a cavity within the body for powering the sweeper head with fluid flow while irrigating the capsular space, aspirating the capsular space, or both. Sweeping a surface of the lens capsule while irrigating facilitates clearing remnants and other material from the capsular space following removal of cataracts or another ophthalmologic procedure.

Abstract: The present disclosure provides systems and methods for transfer of tissue or other materials such as adipose tissue. The systems and methods can include a vessel and a syringe to facilitate transfer of tissue between one or more vessels and tissue implantation devices.

Abstract: Medical fluid management assembly includes: a pneumatic manifold including multiple plates forming pneumatic passageways, a pneumatic valve chamber and a pneumatic pump chamber, the valve chamber in pneumatic communication with at least one passageway, the pump chamber in pneumatic communication with at least one passageway; and a fluid manifold including multiple fluid pathways, a fluid valve chamber in selective fluid communication with a fluid pump chamber and at least one fluid pathway, wherein (a) the pneumatic valve chamber and the fluid valve chamber are mated together to compress a membrane and (b) the pneumatic pump chamber and the fluid pump chamber are mated together to compress a membrane, wherein at least one of the pneumatic valve chamber or the pneumatic pump chamber extends from the at least one plate, or the fluid valve chamber or the fluid pump chamber extends from the fluid manifold to aid in compressing the membranes.

Abstract: A device for intrauterine vacuum therapy includes a pear-shaped fluid-collecting element and a fluid-communicating element. The fluid-collecting element defines an inlet opening at the proximal end and a tubular cavity for receiving a removable guide-rod during transvaginal insertion into a uterine cavity. The fluid-communicating element has a perforated distal end fixed within the fluid-collecting element outside the tubular cavity and has a proximal end adapted for connection to a vacuum-generating system. A method of treating an intrauterine wound or infection includes transvaginally inserting a drain into a uterine cavity and applying a negative pressure to the drain such that the uterus collapses and the inner wall is aspirated against the drain.

Abstract: Methods for adjusting the solubility of a botanical oil in water, along with the resulting modified botanical oil and related products (e.g., treatment compositions, wipes, absorbent articles, etc.) are provided. In one embodiment, the method includes reacting the botanical oil to form a reactive product (e.g., having a hydroxyl group); and attaching a hydrophilic end group (e.g., a carboxylic acid, a carboxylic acid salt, a sugar, etc.) on the reactive product to form a modified botanical oil. The modified botanical oil generally, in most embodiments, has a greater solubility in water than the botanical oil (e.g., a solubility in water of about 10 grams per 100 grams of water or greater, such as completely soluble in water). The botanical oil includes, in one particular embodiment, an essential oil, such as those essential oil that include at least one terpene compound.

Abstract: A device which is used in place of known catheters, such as the Foley catheter, in tests such as a Urodymics test. The device holds the catheter in place.

Abstract: Some illustrative embodiments of an instillation assembly for treating a tissue site may include a fluid distribution lumen and a fluid hub that may define a fluid instillation pathway. The fluid distribution lumen may be defined by a first film layer and a second film layer, and the fluid hub may be positioned in fluid communication with the fluid distribution lumen. The instillation assembly may be used in combination with a reduced-pressure assembly that may define a reduced-pressure pathway separate from the fluid instillation pathway.

Abstract: A tracheal and pharyngeal suction device includes a handle including an interior cavity within the handle body, a connector positioned within the interior cavity and moveable along at least a portion of a length of the interior cavity, a proximal suction catheter having a coupling portion and a treatment portion, wherein the coupling portion is coupled to a proximal side of the connector; and a distal suction catheter coupled to a distal side of the connector.

Abstract: A system for the surface and subsurface delivery of therapeutic and cosmetic agents. The system includes a disposable attachable tip that can be pre-filled with medications or cosmetics and attached to hand pieces including electromagnetic and mechanical energy hand piece devices.

Abstract: A wound dressing for use in the application of negative pressure to a wound, comprising a support member and a cover member positionable over the wound in use. The support member can have a first support element having a first portion aligned with a first axis and a body portion coupled with and extending away from the first portion, and a second support element having a first portion aligned with the first axis and a body portion coupled with and extending away from the first portion of the second support element. At least the body portion of each of the first support element and the second support element can be independently rotatable about the first axis. The support member can support at least a middle portion of the cover member above a surface of the wound so as to define a space between the wound cover and the wound.

Abstract: A system and method for mixing compounds is disclosed. Accordingly to one embodiment a transfer device is provided that allows for diluent from a syringe to be introduced into a container having a first compound (e.g., powder) in a sterile manner. In second and third embodiments, systems are shown for combining and mixing first and second compounds contained in first and second containers in a sterile manner. Various dropper tips for dispensing the mixed compounds are disclosed.