An apparatus for providing negative-pressure therapy may comprise a negative-pressure chamber and a pneumatically-actuated service timer, which can be used to indicate an expiration or other service condition of the apparatus. The apparatus may further comprise an actuator operable to engage a timer fluid with a migration medium. The timer fluid and the migration medium may be selected so that migration time through the migration medium corresponds to an expiration condition of the apparatus. The timer may also provide indicia of migration progress or termination.

The present invention may provide a medical syringe comprising: a cylinder including a stopper protruding inward; and a plunger disposed inside the cylinder so as to move back and forth in a first direction, wherein the plunger includes a plurality of protrusions, and the plurality of protrusions are arranged at intervals along the longitudinal direction of the plunger, and based on the first direction, any one of the stopper or the plurality of protrusions is arranged so as to be selectively overlapped according to the rotation of the plunger.

The present invention provides a manually operated negative pressure wound treatment (NPWT) apparatus for suction of bodily fluids using the negative pressure generated by means of manual pressing. The NPWT apparatus is made of two parts: [1] top functional part; and [2] bottom collector part. The top functional part is made of a pressing mechanism attached to a bellow enclosed within an enclosure. The bellow is connected to the wound dressing using an external medical tube through a one-way check valve, wherein the negative pressure gets created within the bellows when compressed by manually pressing the mechanism. The negative pressure of the bellows sucks the bodily fluid from the wound, which promotes a new blood supply, cleaning infection, and accelerates healing dramatically. The bottom collector part is attached with the bellow through the internal one-way valve, wherein the collector collects the fluid from the bellow when the piston is pressed in the next cycle. Pressure levels and wound conditions are measured and transmitted to the user's smart device, in order to enhance treatment monitoring and efficacy.

This invention relates to the design of tissue covering elements for use in vacuum assisted tissue apposition systems, wherein the geometry of the covering elements favours the application of contractile forces over compressive or extensive forces at the tissue interface.

In some embodiments, a negative pressure wound therapy system can detect and classify one or more operational conditions, including detection of a wound bleeding. The system can react to detection of blood by providing an indication, reducing the intensity or stopping therapy, releasing negative pressure, etc. In certain embodiments, the system can detect one or more additional operational conditions, such as change in vacuum pressure, gas leak rate change, exudate flow rate change, water flow rate change, presence of exudate, presence of water, etc. The system can detect and distinguish between different operational conditions and provide indication or take remedial action.

A negative pressure wound therapy apparatus can include a source of negative pressure configured to aspirate fluid from a wound covered by a wound dressing, a first pressure sensor configured to measure pressure downstream of the source of negative pressure, and a controller configured to, in response to a determination that pressure measured by the first pressure sensor satisfies a threshold indicative of a first blockage downstream of the source of negative pressure, provide an indication of the first blockage. The system can further include a second pressure sensor configured to measure pressure upstream of the source of negative pressure and the controller can be further configured to, in response to a determination that pressure measured by the second pressure sensor satisfies a threshold indicative of a second blockage upstream of the source of negative pressure, provide an indication of the second blockage.

Some embodiments are directed to a system 10 for the application of topical negative pressure therapy to a site 18 on the body of a mammal. Some embodiments of the system 10 comprise a piston 22 and cylinder 24 device 12 having a self-contained power source for the generation of a reduced pressure and for aspirating the site 18. Some embodiments of the system 10 comprise a dressing 14 sealably surrounding the site 18 that can be operably connected to the device 12 by a conduit means 16 to apply the reduced pressure to the site 18.

In one embodiment, system for real time monitoring of catheter aspiration includes a housing having a first port adapted for connection to a vacuum source and a second port adapted for connection with an aspiration catheter, a pressure sensor in fluid communication with an interior of the housing, 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 an alert signal when a deviation in fluid pressure measured by the measurement device exceeds a pre-set threshold. In another embodiment, the system for real time monitoring of catheter aspiration further includes a vacuum source for connection to the first port and an aspiration catheter having an aspiration lumen for connection to the second port.

A composite wound dressing apparatus promotes healing of a wound via the use of a micropump system housed within or above a wound dressing member. The micropump system includes a miniature pump that applies a subatmospheric pressure to the wound to effectively draw wound fluid or exudate away from the wound bed without the need for a cumbersome external vacuum source. Hence, the wound dressing and micropump system is portable which allows the patient mobility that is unavailable when an external vacuum source is used. The patient does not need to be constrained for any period of time while exudate is being removed from the wound.

Embodiments disclosed herein are directed to a drainage control system including, a tubular body with a tubular body lumen extending from a distal end to a proximal end and a collapsible tube disposed within the tubular body lumen, the collapsible tube including a collapsible tube lumen extending from a distal end to a proximal end of the collapsible tube. The collapsible tube can be attached to the tubular body, such that fluid flow through the tubular body lumen flows through the collapsible tube lumen. The tubular body can include a valve that is actuatable between a first configuration wherein fluid flow is allowed through the tubular body lumen and a second configuration wherein fluid flow is prevented through the tubular body lumen. An airflow source can be coupled to the valve such that pressure from the airflow source actuates the valve.