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.

Systems, apparatuses, and methods for providing negative pressure to a tissue site are closed. Illustrative embodiments may include a system comprising a dressing having tissue interface in fluid communication with the tissue site. Such system may also comprise a canister having a fluid inlet fluidly coupled to the canister and an ambient inlet fluidly coupled to ambient air outside the collection chamber. Such system may further comprise a first outlet fluidly coupled to the canister and adapted to receive negative pressure from a source of negative pressure, and a second outlet. Such system also may comprise a fluid conductor fluidly coupled between the second outlet and the tissue interface, wherein the fluid conductor may be adapted to deliver ambient air to the tissue site. In some embodiments, such system may also comprise a regulator fluidly coupled between the second outlet and the ambient inlet, wherein the regulator is adapted to provide ambient air through the fluid conductor to the tissue site in a controlled fashion.

An apparatus is including a negative pressure wound therapy pump including a pump housing; and a negative pressure wound therapy canister attached to and readily removable from the pump housing; the canister including a flexible conduit; the canister operable to receive suction generated by the pump; the flexible conduit sized, shaped, and located to interface with the pump housing of the pump such that suction produced by the pump is transmitted to the canister via the flexible conduit.

A liquid-collection canister includes a liquid collection chamber defined by at least one wall and a first and second gas-communication pathway formed within the at least one wall. A first aperture is positioned between the first gas-communication pathway and the liquid collection chamber to allow gaseous communication between the liquid collection chamber and the first gas-communication pathway. A second aperture is positioned between the second gas-communication pathway and the liquid collection chamber to allow gaseous communication between the liquid collection chamber and the second gas-communication pathway. A first and a second liquid-air separator are positioned over the first aperture and the second aperture, respectively, to substantially prevent liquid passing through the first and second apertures.

A wound fluid collection system includes a canister with a chamber fluidly connected to a wound dressing in a tissue site through an inlet and also fluidly connected to a reduced pressure source through an outlet. At least a portion of the canister is collapsible and yet can be maintained in an extended state when exposed to subatmospheric pressure. The canister is releasably attachable to a supporting member.

In some examples, provided is a fluid blockage device for use with a reduced-pressure source for treating a tissue site with reduced pressure. The fluid blockage device may be configured to preclude fluid communication through a port fluidly coupled to the reduced-pressure source when the fluid blockage device contacts a liquid. Other devices, systems, and methods are disclosed.

A wound therapy system includes a single conduit fluidly connecting a wound site to a. removed fluid canister. A negative pressure circuit is defined by the wound site, the conduit, the removed fluid canister and tubing extending between the removed fluid canister and a pneumatic pump that applies negative pressure to the negative pressure circuit. A method of operating the wound therapy system includes profiling and benchmarking pressure decay within the negative pressure circuit against previous and/or expected pressure decay to identify any new or sudden anomalies that occur during the operation of the wound therapy system. The wound therapy system may additionally alert a user to such anomalous operation of the wound therapy system and/or identify and alert a user to an underlying cause (e.g, blockage and/or leak, etc.) that is responsible for the anomalous readings.

A system and apparatus for the collection of serous or serosanguinous fluid from a percutaneous site after surgery. A pump unit with one or more pumps or powered sources provide continuous negative pressure suction to draw fluid from the percutaneous site and pumps the fluid into disposable reservoirs with one-way valves that are easy to handle while maintaining sterility and a seal to prevent the loss of vacuum. Air is continuously removed from the reservoirs. Measurement and analysis of the output is performed automatically. Additionally, through such a peristaltic pump device, controlled collection of measured surgical and/or bodily fluid from a subject patient may be undertaken allowing for more effective and closer analysis, as well.

Provided is a container for connection to a device for suctioning bodily fluids and for supplying a fluid substance to a human or animal body said container comprising an interior which is divided into a first region for collecting the suctioned bodily fluids and into a second region for providing the fluid substance The first region of the interior is separated from the second region by means of a flexibly realized partition wall

In some examples, provided is a fluid blockage device for use with a reduced-pressure source for treating a tissue site with reduced pressure. The fluid blockage device may be configured to preclude fluid communication through a port fluidly coupled to the reduced-pressure source when the fluid blockage device contacts a liquid. Other devices, systems, and methods are disclosed.