The illustrative embodiments described herein are directed to a manually-actuated pump and method for applying reduced pressure at a tissue site. The manually-actuated pump includes at least one variable volume chamber that is manually compressible into a plurality of positions. The manually-actuated pump includes a fixed volume chamber in communication with the at least one variable volume chamber. The manually-actuated pump also includes a filter housing having a hydrophobic filter that prevents liquid from entering the at least one variable volume chamber. The fixed volume chamber is coupled to the at least one variable volume chamber via the filter housing. The filter housing is located in between the at least one variable volume chamber and the fixed volume chamber. The fixed volume chamber has reduced pressure that is applied to the tissue site in response to a movement of the at least one variable volume chamber from a compressed position in the plurality of positions to an uncompressed position in the plurality of positions.

Manifold for a medical/surgical waste collection assembly. A shell includes a proximal end base, and a lip extending proximally from the proximal end base. The lip extends around an outlet opening defined in the proximal end base that is off-centered to a longitudinal axis of the shell. A cap including a cap head is coupled to a side wall of the shell. A drip stop may be seated within a space defined by the lip to cover the outlet opening. An arcuate section of the lip may be flush with an adjacent section of the side wall. The cap head may define a through hole, and a flapper valve unit may be coupled to the cap head with another component having ears extending through the through hole. A fence may extend from the cap head and configured to be grasped by a user.

A method and apparatus are disclosed for determining status of a canister of a topical negative pressure (TNP) system. The method includes the steps of monitoring pressure provided by a pump element of the TNP system, determining at least one characteristic associated with the monitored pressure and determining status of at least one parameter associated with a canister of the TNP system responsive to the determined characteristics.

Apparatuses for use in negative pressure wound therapy are described herein. In some embodiments, the apparatus includes a pump assembly having a pump housing, a magnet, an electrically conductive coil, and a diaphragm, wherein the electrically conductive coil is configured to move a portion of the diaphragm to pump a fluid through the pump apparatus, and a dampener positioned within the pump assembly configured to reduce sound generated by the pump assembly during operation of the pump assembly. In some embodiments, the apparatus includes a housing having a first section and a second section, and an illumination source disposed within the housing adjacent the first section, wherein the illumination source is configured to illuminate the first section, wherein the first section is one of transparent and translucent, and wherein the first section is thinner than the second section as measured perpendicularly from inside to outside the housing. In some embodiments, the pump apparatus includes components configured to be laser welded together.

A dressing for treating a tissue site with negative pressure may include a core having a first surface, a second surface, and an absorbent between the first surface and the second surface, a cover disposed over the first surface of the core, a pressure indicator configured to change shape under negative pressure, and a fluid conductor coupling the pressure indicator to the second surface of the core.

A system for real time monitoring of catheter aspiration includes a pressure sensor configured for placement in fluid communication with a lumen which at least partially includes an aspiration lumen of a catheter, the aspiration lumen configured to couple to a vacuum source, a measurement device coupled to the pressure sensor and configured for measuring deviations in fluid pressure, and a communication device coupled to the measurement device and configured to generate a continuous signal which is proportional to measured fluid pressure.

A reduced pressure treatment system is provided that includes a canister that is fluidly connected to a tissue site and is configured to receive fluid drawn from the tissue site under the influence of a reduced pressure. A reduced pressure source provides the reduced pressure and is fluidly connected to the tissue site by a fluid communication path, which may include a source conduit, the canister, and a target conduit. A sensing device communicates with the source conduit and is configured to sense a pressure in the source conduit. A valve communicates with the source conduit and is configured to vent the reduced pressure. A processing unit communicates with the sensing device and the valve and is configured to open the valve for a selected amount of time, determine a decay of reduced pressure, and determine a fill status of the canister based on the decay of reduced pressure.

Embodiments of a negative pressure wound therapy systems and methods for operating the systems are disclosed. In some embodiments, a system includes a pump assembly, canister, and a wound dressing configured to be positioned over a wound. The pump assembly, canister, and the wound dressing can be fluidically connected to facilitate delivery of negative pressure to a wound. The pump assembly can present graphical user interface screens for controlling and monitoring delivery of negative pressure. The system can be configured to efficiently deliver negative pressure and to detect and indicate presence of certain conditions, such as low pressure, high pressure, leak, canister full, and the like. Monitoring and detection of operating condition can be performed by measuring one or more operational parameters, such as pressure, flow rate, and the like.

A reduced-pressure device for wound treatment includes a housing, an air pressure storage unit, a compression unit and a pressure indicating module. The air pressure storage unit is installed in the housing and comprises a pressure storage container, a piston assembly and a piston spring, and the compression unit is mounted on the piston assembly, and the pressure indicating module is engaged to the pressure storage container and the piston assembly. Therefore, the user can see the information shown on the pressure indicating module to be easily aware of how much capacity of negative pressure the reduced-pressure device can continuously be provided in order to determine when to operate the compression unit again for providing the desired negative pressure.

A method and apparatus for fluid removal from a patient includes a disposable fluid removal subassembly and a portable drive subassembly that manage controlled extraction of a fluid from a patient. The fluid removal subassembly is configured for accessing a fluid filled cavity of a patient and also coupled with a fluid flow inducer having an inflow fluid intake and an outflow fluid output. The entire fluid removal subassembly, inclusive of a connector, a fluid conduit, and the fluid flow inducer, but exclusive of the outflow fluid output and a collection bag, is fluidly sealed from an external environment, and un-vented to the external environment. The fluid removal system enables a closed-loop fluid path between the patient through to the fluid flow inducer, which is under direct control by the patient of flow rate and therefore resulting pressure in the fluid path.