A neurovascular catheter extension segment is provided, such as for distal neurovascular access or aspiration. The neurovascular catheter extension segment includes 1) an elongate flexible control wire having a proximal end and a distal end and 2) a tubular extension segment having a side wall defining a central lumen carried by the distal end of the control wire. The side wall of the tubular extension segment includes a tubular inner liner, a tie layer separated from the lumen by the inner liner, a helical coil surrounding the tie layer, and an outer jacket surrounding the helical coil. The extension segment may be introduced into the proximal end of a neurovascular catheter and advanced distally to extend beyond the catheter and thereby extend the reach of the catheter.

A waste collection unit including a waste container, and vacuum source to collect medical waste into the waste container. The vacuum source is disposed within a sound attenuating enclosure that defines an enclosure inlet for receiving cooling air and an enclosure outlet for discharging warmed cooling air. The sound attenuating enclosure is at least partially formed of a sound-absorbing material and may define a pocket for receiving a first end of the vacuum source. The first end of the vacuum source may engage a seat of the sound attenuating enclosure to provide a cooling air barrier. The seat may define a bottom portion of the pocket. Internal geometries of the sound attenuating enclosure may be shaped to define another air path that does not pass through the vacuum source. A plenum may be attached to the sound attenuating enclosure and define a plenum chamber to collect the warmed cooling air.

A method of irradiating a wound that includes positioning a wound insertion foam within a wound cavity of a wound and covering the wound insertion foam using a wound sealing layer. The method further includes pumping fluid from the wound cavity using a drain tube sealed within the wound cavity and coupled to a vacuum source, and irradiating the wound using a light diffusing optical fiber that is optically coupled to a therapeutic light source and includes light scattering structures distributed along the light diffusing optical fiber. A portion of the light diffusing optical fiber is positioned within a wound tissue region of the wound, the wound cavity, or both, such that light emitted by the therapeutic light source enters the light diffusing optical fiber, scatters outward from the light diffusing optical fiber, and irradiates the wound tissue region, a wound cavity surface of the wound, or both.

An example breast pump system can include: a control unit including a processor and memory, the control unit including an interface to control the breast pump system; a vacuum unit controlled by the control unit, the vacuum unit including pump motors to create suction for pumping milk; a support mechanism located remotely from the control unit; and a member extending between the control unit and the support mechanism, the member being movable to allow the control unit to be repositioned relative to the support mechanism. The memory encodes instructions which, when executed by the processor, cause the breast pump system to: select at least a first pump motor from the plurality of pump motors for a first pumping timeframe; and select at least a second pump motor from the plurality of pump motors for a second pumping timeframe.

A drainage system includes a vacuum chamber to receive drainage liquid from a drainage tube. The chamber can include an input port coupled with the drainage tube and a drain port coupled with a collection container. The system can include an air pump having an input coupled with a vacuum port of the vacuum chamber and a distal end of the drainage tube. Activation of the air pump can establish circulating fluid flow between the drainage tube and the vacuum chamber, and deactivation of the air pump can permit drainage liquid to drain from the vacuum chamber into the output tube. Also disclosed is a method of draining liquid from a patient, including accumulating a volume of the drainage liquid at a first location along a drainage pathway, moving the volume to a second location, accumulating the volume at the second location, and moving the volume to a collection container.

A negative pressure therapy system is provided for inducing negative pressure in a portion of a urinary tract, the system including: (a) at least one ureteral catheter configured to be positioned within a ureter and/or kidney; (b) one or more sensor(s) configured to determine information about at least one of blood composition, blood flow, respiration, heart rate, glucose, protein, or creatinine; and (c) a controller configured to increase urine production by adjusting one or more operating parameters of a negative pressure source for inducing negative pressure through the at least one ureteral catheter into the urinary tract, based at least in part upon the information determined by the one or more sensor(s).

Embodiments of 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 also include a transmitter configured to communicate with a remote computing device when the pump assembly is within a coverage area of the remote computing device, enabling the remote computing device to determine whether the housing is within the coverage area.

The invention is directed to an ophthalmosurgical system which includes a console for accommodating an irrigation fluid vessel containing irrigation fluid and a cassette, insertable into the console, for directing the irrigation fluid to a surgical instrument for an eye to be treated. An irrigation fluid flow path leads from the irrigation fluid vessel to the cassette and to the surgical instrument. A first fluid pump includes a first pump chamber having a first volume and a first drive chamber separated therefrom by a first elastic partition and having a second volume. A second fluid pump is arranged in parallel to the first fluid pump and includes a second pump chamber having a third volume and a second drive chamber separated therefrom by a second elastic partition and having a fourth volume. The first volume or the third volume has a magnitude within the range from 1 to 25 cm.sup.3.

A breast pump assembly is disclosed. The breast pump assembly according to an aspect of the present disclosure may include: a breast pump including a contact housing with a backside recessed to wrap a breast and a storage housing coupled to the contact housing to define a breast milk storage space on a frontside of the contact housing, the breast pump being provided with a coupling cavity penetrating an upper portion of the storage housing; a stopper detachably coupled to the coupling cavity and provided with a first air pipe connector; an air pipe coupled to the first air pipe connector; and a pump cradle provided with a second air pipe connector to which the air pipe is coupled, wherein the pump cradle includes: a first case provided with the second air pipe connector, an insertion hole and an air passage connector; a first milking pump installed in the first case; a duct connecting the first milking pump and the air passage connector to the second air pipe connector; and a pump module including a second case detachably coupled to the insertion hole and a second milking pump installed in the second case, wherein the second case is provided with an air passage connecting the air passage connector with the second milking pump, and wherein the pump module is separated from the insertion hole and detachably coupled to the coupling cavity from which the stopper is separated.

A fluid management system including a pass-through fluid volume measurement system to provide continuous measurement of fluid returned from a surgical site during transit to a waste collection system. The pass-through fluid volume measurement system eliminates the need to physically replace full fluid collection containers during the medical procedure with new, empty fluid collection containers.