Abstract:
A system for managing reduced pressure to a wound site includes a wound enclosure configured to form a substantially sealed volume around the wound site, a first closed volume, a second closed volume, and a controller. The first closed volume includes a primary pressure source and a canister fluidly coupled to the primary pressure source. The first closed volume is configured to apply reduced pressure to the wound site and deliver exudate collected from the wound site to the canister through a first lumen. The second closed volume includes a secondary pressure source and is configured to apply a secondary pressure to the wound site through a second lumen to facilitate flow of the exudate from the wound site to the canister through the first lumen. The controller is configured to communicate with at least the second closed volume for selectively applying the secondary pressure to the wound site.
Abstract:
Variables of a surgical system are detected or received via one or more sensors to predict an intraocular pressure (IOP) and/or determine an IOP in real time during a surgical procedure. A notification to a surgeon or a target IOP is set and maintained as determined by Static IOP, dynamic IOP, and/or a total IOP combining both static and dynamic IOP of the anterior chamber of a patient's eye. Information collected about various components of the system are displayed on a user interface. The system uses the collected information to calculate the static IOP and/or dynamic IOP of the system, and the total IOP may be function of the static IOP and/or dynamic IOP measurements.
Abstract:
Embodiments include a vacuum assisted venous drainage (VAVD) system, including a regulator valve assembly configured to facilitate application of vacuum to a reservoir; a control unit configured to control the regulator valve assembly to facilitate controlling application of the vacuum; at least one pressure sensor coupled to the reservoir and configured to obtain pressure measurements of pressure in the reservoir; a heating element configured to heat the regulator valve assembly to a target temperature; and at least one temperature sensor configured to determine a temperature of the regulator valve assembly.
Abstract:
A system for removing occlusive clot from a blood vessel comprises a catheter and an apparatus for generating a pulsatile vacuum force to pulse the pressure gradient at a distal end of the catheter. The pulse generator may be integral with or separate from the vacuum pump. The pulse generator may be applied to a flexible tubing between the vacuum pump and the proximal end of the catheter.
Abstract:
The present invention relates to a pump arrangement (1) for a double breast pump (2). The pump arrangement (1) comprises first and second terminals (23, 24) for connecting first and second expression kits (3, 4) having first and second breast shields (5, 6) and at least one container (7) for collecting breast milk (8) in fluidic connection with the expression kits (3, 4), a pump (9) for generating reduced pressure within said breast shields, a plurality of conduits (10, 11, 14, 15, 16), a suction valve (12) connected to the pump (9) by a connection conduit (14) and to the first and second terminals (23, 24) by respective air conduits (10, 11), and a venting valve (13) connected to the first and second terminals (23, 24) by venting conduits (15, 16), wherein the venting valve (13) comprises an opening (17) to the environment. The pump (9) is alternatingly connected to the first and second terminals (23, 24) by alternate opening and closing of the suction valve (12) and the venting valve (13).
Abstract:
Systems, devices, and methods of the present disclosure assist with management of tubes and hoses during surgical procedures. The systems, devices, and methods provide for the proper opening and closing of tubes to facilitate performance of steps in a surgical procedure. Systems, devices, and methods of the present disclosure control fluid delivery to and from a medical device, including devices for tissue processing and cleaning.
Abstract:
A suction device is shown and described. The suction device includes a body, an input port configured to receive a flow of matter, a suction port, and a suction lumen that couples the suction port to the input port. In some embodiments the suction device is configured to couple with a surgical instrument for use in a surgical procedure.
Abstract:
This patent document discloses assemblies and methods for removing obstructive material from a body vessel or other cavity. An assembly can include an elongate inner member, an elongate outer member, an aspirator, one or more valves, and a waste collection reservoir. Each of the elongate members can extend from a proximal end portion to a distal end portion and can include a lumen therethrough. The elongate inner member can be partially disposed in the lumen of the elongate outer member and can be moveable along its longitudinal axis relative to the elongate outer member. The aspirator can be in flow communication with the proximal end portion of the elongate inner member for drawing the obstructive material into or through its lumen. The one or more valves can be configured and positioned to allow obstructive material removed from the body vessel or cavity to be urged toward the waste collection reservoir.
Abstract:
A bone dust collection device includes a bone dust collection structure defining a longitudinal axis and having a proximal end and a distal end. The bone dust collection structure has a transverse plate member connected at or in the vicinity of the proximal end to a cylindrical wall defining an aperture at the distal end for receiving and collecting bone dust. The aperture extends proximally and includes a filtration member disposed therein. The filtration member causes at least partial separation of fluid from the bone dust via the fluid passing proximally through the filtration member. The bone dust collection structure enables removal of bone dust collected therein. A method of collecting an anatomical specimen includes generating an anatomical specimen in particulate form at a surgical site of a subject; collecting the particulate accumulated in the collection device; and packing the collected particulate into a region of interest in the subject.