Disclosed cannula systems can detect the tissue type within which the cannula tip is located in real time using electrodes adjacent the cannula tip. The sensing cannula system can differentiate when the cannula tip is in adipose tissue or muscle based on electrical impedance. The system can be used in fat grafting and liposuction procedures, for example. An operator can detect if the cannula tip enters muscle by watching for an indicator light or audible alarm that is automatically activated by the device based on a change in sensed impedance. The device may also stop the flow of fat through a pump halting injection into the sub-muscular space.

The present patent specification provides a medical device including an outer tube, an operation portion and a control portion. The operation portion is at least partially located in the outer tube. The control portion has a channel communicating with the outer tube along a first direction; a second end of the control portion is coupled with a first end of the outer tube so that the channel and the outer tube communicate with each other along the first direction. The control portion includes a control module including a suction control unit, a suction, a suction valve actuator and a switching unit. The suction control unit has a stopping unit and is configured to move along a second direction which is different from the first direction. The suction valve actuator is located at a side opposite the suction control unit with the channel therebetween and the suction valve actuator is configured to be activated by the suction control unit. The switching unit is configured to switch the work status of the operation portion.

In one embodiment, a fluid dynamics system includes a solenoid valve including a valve body, which includes a valve cavity having a direction of elongation, a first channel, and a second channel, a solenoid coil disposed in the valve body around the valve cavity, and a plunger comprising a magnetic element and configured to move back-and-forth along the direction of elongation between a first position and a second position in the valve cavity, selectively opening the first channel and closing the second channel when the plunger is in the first position, and closing the first channel and opening the second channel when the plunger is in the second position, and a controller configured to control the solenoid coil to selectively move the plunger between the first position and the second position, and to selectively maintain the plunger in the first position and the second position.

An evacuation system and method for removing and/or treating gaseous and/or particulate byproducts of surgical procedures includes an end effector such as a side vent trocar, an operating room tower or the equivalent, a disposal vessel, a vacuum source and optionally a filter. The end effector may be coupled to the tower by a conduit, the tower may be coupled to the collection tank by a conduit, and the collection tank may be coupled to the vacuum source. Gaseous and/or particulate byproducts may flow from the surgical site through the trocar, conduits, tower tank and filter, and the flow may be regulated at least in part by the components of the system.

An endoscopic system may include an endoscope including a handle and an elongate shaft extending distally from the handle, wherein the handle includes an inflow port in fluid communication with the elongate shaft, the inflow port being configured to fluidly connect to a fluid inflow line, an electronically adjustable orifice associated with the inflow port, and control circuitry for receiving a signal of a current size of the electronically adjustable orifice and/or for sending a signal to change a size of the electronically adjustable orifice. The system may include a first pressure sensor disposed upstream of the electronically adjustable orifice and a second pressure sensor disposed downstream of the electronically adjustable orifice.

A portable suction pump for aspirating secretions from a patient's artificial airway includes a peristaltic pump head, a suction tube extending from a patient through the peristaltic pump head, the suction tube having a tee-fitting conduit, and a collection container having a plurality of ports for collecting patient media. A clinician has an ability to increase or decrease vacuum levels without increasing or decreasing flowrate and/or an ability to increase or decrease the flow rate without increasing or decreasing the vacuum levels. The tee-fitting conduit extends to a vacuum sensor port connecting to a vacuum sensor in communication with a processor, the processor controlling a proportional valve employed to regulate the vacuum levels.

A suction and irrigation valve for a robotic surgical system includes a shaft assembly, a rotary drive, and a valve assembly. The valve assembly is operatively connected to the rotary drive member and includes a valve body and a valve plug. The valve body has a first fluid inlet, a second fluid inlet, and an outlet. The valve plug is received with the valve body and is configured to rotate about a plug axis relative to the valve body to a first position, a second position, and a third position. The valve plug has at least a first conduit configured to selectively fluidly communicate with each of the outlet and at least one of the first or second fluid inlets.

Embodiments of negative pressure wound therapy systems and methods for operating the systems are disclosed. In some embodiments, a system includes a pump assembly and a wound dressing configured to be positioned over a wound. The pump assembly and the wound dressing can be fluidically connected to facilitate delivery of negative pressure to a wound via a fluid flow path. The system can be configured to efficiently deliver negative pressure and to detect and indicate presence of conditions, such as a blockage in a fluid flow path. Monitoring of the conditions can be performed by detecting a level of activity of a pump of the pump assembly.

A method for aspirating thrombus in a subject, the method including providing an aspiration catheter having a supply lumen, an aspiration lumen, and a first connector hydraulically coupled to the aspiration lumen. The method further includes providing a pressure sensor having an internal passageway and having a distal connector configured to hydraulically couple to the first connector, a proximal connector configured to couple to a vacuum source, and a valve disposed between the distal connector and the proximal connector, the valve having an open state and a closed state. Following inserting at least a distal portion of the aspiration catheter into the vasculature of a subject, changing the valve from one of the open state and closed state to the other of the open state and closed state such that a change in pressure may be detected by the control circuitry.

A system for aspirating thrombus that includes an aspiration catheter, a tubing set connected to the aspiration catheter, a pressurization element configured to couple to the tubing set and further configured to pressurize fluid from a first fluid source or allow pressurized fluid from the first fluid source to be transferred through a supply lumen of the aspiration catheter, and a sheath through which the aspiration catheter can be advanced.