A negative pressure wound therapy device that includes a first tubing connectable in flow communication with a source of negative pressure configured for application of negative pressure to a wound site, a second tubing in flow communication with the wound site, and a valve.

A system for connection to a catheter to aspirate clot from the vasculature of a patient includes a vacuum console and a canister assembly which can be removably mounted in a mounting region of the vacuum console. The canister assembly includes a clear canister with an interior and an open top. A lid is removably attachable over the open top of the clear canister, and the clear canister has a vacuum port and a pressure sensing port each formed in a wall of the canister. The vacuum port aligns with a vacuum connector on the enclosure and the pressure sensing port aligns with a pressure sensing connector on the enclosure when the canister assembly is mounted on the mounting region of the vacuum console. The clear canister has a filter plate configured to be suspended in the interior of the clear canister at a location mid-way between the open top and a bottom to separate clot from blood as they are aspirated from the catheter.

A therapy system for treating a tissue site with negative-pressure therapy and/or fluid instillation therapy in response to information received from a diagnostic module is disclosed. In some embodiments, the therapy system may include a dressing, a negative-pressure source, a container, and a diagnostic module. The dressing may be adapted to be placed on the tissue site, and the negative-pressure source may be adapted to be fluidly coupled to the dressing. The container may be adapted to be fluidly coupled to the dressing and to the negative-pressure source and to receive fluid from the tissue site. The diagnostic module may be adapted to be exposed to gas associated with the fluid from the tissue site. The diagnostic module may comprise a sensor configured to detect a condition of the tissue site and to generate an output based on the detected condition. The sensor may be configured to detect a volatile organic compound. In some embodiments, the diagnostic module may be positioned on the container.

Disclosed herein are various techniques and devices for detecting a level of fluid within a fluid collection receptacle. In one embodiment, a pressure sensor connected to a bottle is provided. The pressure sensor detects air pressure in the bottle as the bottle is filled with a liquid and provides information to determine a volume of the liquid in the bottle.

A surgical drape adapted to overlay a patient including an opaque sheet having superior region extending to a cephalad end with a fenestration configured to surround a surgical region of the patient, and an inferior region extending from the inferior aspect of the fenestration to a caudal end and having a transparent sheet joined to the patient facing side of the opaque sheet proximate the inferior aspect of the fenestration between opposite opaque sheet first and second edges allowing the inferior portion of the opaque sheet drawn away from the transparent sheet to allow a surgeon visual access to the patient through the transparent sheet.

A suction stent for introduction into a hollow organ of the human or animal body, preferably into the gastrointestinal tract, in particular the intestine, includes a tubular hollow body which is open in the longitudinal direction and made of biocompatible material. The tubular hollow body has a fixed diameter at least in its central portion; and a porous shapeable material, preferably a sponge material, which is biocompatible and shapeable in the radial direction, the porous shapeable material radially sheathing the tubular hollow body at least in a section of the tubular hollow body. Further, a method is provided for sealing a leakage, especially an anastomosis, of the hollow organ.

Systems and methods for estimating a blood volume within a canister. The system may include means for detecting a fluid level of the fluid, such as a float sensor mechanism disposed within the canister. An imaging device captures an image of the fluid within the canister. A processor determines an estimated concentration of a blood component in the fluid based on the image. The processor determines a canister volume of the fluid based on the detected fluid level, and estimates the blood volume within the canister based on the estimated concentration of the blood component and the determined canister volume. The processor may trigger the imaging device to capture the image based on a change in the canister volume. An insert may be arranged within the canister and positioned adjacent to and offset from a transparent region of the canister.

Apparatuses for multi-orientation fluid management are described. In some example embodiments, an apparatus for managing fluids may comprise an absorbent core and one or more layers of a fluid acquisition and manifolding material. The fluid acquisition and manifolding material can provide a shell or envelope for capturing the fluid and distributing it to the absorbent core for storage. The manifolding material can distribute fluid as the absorbent core swells. The apparatus may additionally include an exudate container providing a casing for the absorbent core and the fluid acquisition and manifolding layers.

Provided herein are kits, devices and methods for rapid analysis of biological samples. In particular, kits, devices and methods described herein can be applied to rapid nucleic acid analysis of solid tissue samples.

An example urinary collection device includes a fluid impermeable barrier defining a chamber, an opening, and an outlet. The opening and the outlet fluid to enter and leave the chamber, respectively. The urinary collection device also includes a fluid permeable membrane extending across the opening. The urinary collection device includes a fluid receiving portion that includes the portions of the fluid impermeable barrier that defines the opening. The fluid receiving portion is configured to be positioned such that the opening is disposed adjacent to the urethral opening of the individual (e.g., a buried penis). The urinary collection device also includes an longitudinal portion extending from the fluid receiving portion. The longitudinal portion is configured to be positioned adjacent to or near the perineum of the individual (e.g., positioned between the thighs of the individual).