A negative pressure wound therapy device includes a piezoelectric pump, a state detector configured to detect a state of the pump, and a control circuit configured to transmit a first control signal for a first period having a first RMS voltage greater than or equal to a threshold voltage at which driving the pump for a second period greater than the first period can cause the pump to emit sound at a magnitude greater than a sound threshold; receive a first indication of the state; determine if the pump is in a leak condition; transmit, responsive to the pump not being in the leak condition, a second control signal having a second RMS voltage less than the first RMS voltage; and transmit, responsive to the pump being in the leak condition, a third control signal having a third RMS voltage greater than the second RMS voltage.

A system for negative pressure and hypoxic tissue therapy including a chemical pump assembly, a dressing to cover a tissue site, a plurality of hoses, and a cover layer to cover a portion of the dressing. Each hose is configured to fluidly connect the dressing to the assembly. Oxygen flows from the dressing to a reactor in the assembly where the oxygen is consumed by the reactor. The hoses have different cross-sectional areas and selectable lengths, and these can be selected to provide a desired amount of oxygen around the tissue site. The cover layer has less permeability to air that does the dressing, nd can be used to cover a portion of the dressing to inhibit the permeation of air through the dressing and thus provide the desired amount of oxygen around the tissue site.

A phacoemulsification system includes a hollow needle, an aspiration line, and a protection valve inserted in the aspiration line. The needle is configured to emulsify a lens of an eye. The aspiration line is for evacuating material from the eye. The protection valve includes a chamber, a piston and a seal. The chamber has an inlet for receiving the material arriving from the needle, and an outlet for flowing the material along the aspiration line. The piston is configured to move in the chamber between a first position that enables material flow between the inlet and the outlet, and a second position that blocks the material flow. The seal is coupled with the inlet and is configured, when the piston is in the second position, to compress between the piston and the inlet in response to a pressure pulse that propagates in the aspiration line, thereby hermetically sealing the inlet.

A wearable defibrillator includes one or more environmental sensors including an accelerometer, one or more ECG sensors configured to acquire ECG data, and an alarm manager and at least one processor operatively coupled to the one or more ECG sensors and the accelerometer. The at least one processor is configured to detect a cardiac abnormality in the patient, identify a notification having one or more characteristics, and detect an environmental condition of the wearable defibrillator. The accelerometer is configured to detect a presence or lack of patient motion, and/or detect a body position of the patient as the detected environmental condition. The at least one processor is configured to determine whether one or more factors exist that inhibit the patient's ability to recognize the notification, on determining their existence, adapt the one or more characteristics of the notification and provide an adapted notification, and issue the adapted notification.

Systems, methods, and apparatuses for irrigating a tissue site are described. The system can include a tissue interface and a sealing member configured to be placed over the tissue site to form a sealed space, and a negative-pressure source fluidly coupled to the sealed space. The system includes an irrigation valve having a housing, a piston disposed in the housing, a fluid inlet to fluidly couple a fluid inlet chamber to a fluid source, and a fluid outlet to fluidly couple a fluid outlet chamber to the sealed space. A piston passage extends through the piston and fluidly couples the fluid inlet chamber and the fluid outlet chamber, and a biasing member is coupled to the piston to bias the irrigation valve to a closed position. The negative-pressure source is configured to move the piston between the closed position and an open position to draw fluid to the sealed space.

A pressure-controlling device (10) includes a pump (21), a connection pipe (30), a first valve (41), and a second valve (42). The pump (21) has an inlet port (211) and an outlet port (212). The connection pipe (30) has a first end in communication with the outlet port (212), and a second end in communication with the inlet port (211) and that has a first space (31) that contains the first end, a second space (32) that contains the second end, and a third space (33) that is located between the first space (31) and the second space (32).

A surgical suction device (10) comprising:

a connector (12),

a surgical cavity insertion tube (14), and

a suction tip (16),

wherein the surgical cavity insertion tube (14) is connected at a proximal end thereof to the connector (12) and at a distal end thereof to the suction tip (16). The suction tip (16) comprises an inner hollow shaft (18) and an outer hollow shaft (20) coaxial to each other, the inner hollow shaft (18) having a first central opening (22) at a distal end thereof, and the outer hollow shaft (20) having an end wall (24) at a distal end thereof, wherein the end wall (24) has a second central opening (26) in axial alignment with the first central opening (22) of the inner hollow shaft (18). The outer hollow shaft (20) has one or more openings (28) on a lateral wall (30) thereof.

In general, devices, systems, and methods for arthroscopic pump saline management are provided. In an exemplary embodiment, a pump system including a pump is configured to manage fluid pumped by the pump to a surgical site during performance of a surgical procedure. The pump system being configured to manage fluid pumped to the surgical site can allow the pump system to manage fluid pressure at the surgical site by monitoring fluid loss at the surgical site.

A mobile negative pressure wound therapy (NPWT) device is described having an inlet; a canister in fluid flow connection with the inlet; a pump having a pump casing with a pump inlet in fluid flow connection with the canister in the canister, and a pump outlet for output of air transported through the pump; an elastomeric jacket at least partly enclosing the pump, the elastomeric jacket being configured to define a flow channel having a first end arranged to receive air output by the pump outlet and a second end spaced apart from the first end for discharging the air output by the pump outlet following passage through the flow channel; a control unit for controlling operation of the mobile NPWT device; a battery arrangement for powering the mobile NPWT device; and a housing enclosing at least the pump, the elastomeric jacket, the control unit, and the battery arrangement.

The present disclosure generally relates to a mobile negative pressure wound therapy (NPWT) device comprising a negative pressure pump, where the NPWT device is adapted to ensure that an operation of the negative pressure pump is terminated if the NPWT device is operating outside of a predefined operational range. The present disclosure also relates to a corresponding method for operating such an NPWT device and a thereto related computer program product.