A system for aspirating thrombus includes a catheter having a supply lumen having a distal end and an aspiration lumen configured to couple to a vacuum source and having an interior wall surface and an open distal end, an orifice at or near the distal end of the supply lumen, in fluid communication with the interior of the aspiration lumen, the orifice located proximally of the open distal end of the aspiration lumen, wherein the orifice is configured to create a spray pattern that impinges on the interior wall surface of the aspiration lumen when a distal end of the aspiration catheter is immersed within an aqueous environment, and a disposable tubing set having a first conduit configured to couple the supply lumen of the aspiration catheter to a fluid source, and a pump component associated with the first conduit and configured to detachably couple to a drive unit.

A catheter that includes a mechanism for deflecting a distal portion of a catheter may include a deflection knob including a first thread, a rod including a second thread that is coupled to the first thread, and a puller wire that is connected to the rod. The rod may additionally include a pocket to which the puller wire may be connected via a joining feature that may be secured in the pocket and attached to a proximal end of the puller wire. The joining feature may include a first ferrule joined, e.g., crimped, to the proximal end of the puller wire and a second ferrule secured, e.g., bonded, in the pocket and joined, e.g., crimped, to the first ferrule.

A bridge for facilitating delivery of reduced pressure to a wound site of a patient includes a reduced pressure lumen configured to be fluidly coupled to a reduced pressure source, and a secondary pressure lumen configured to be fluidly coupled to a secondary pressure source at a first end and to the reduced pressure lumen at a second end, thereby facilitating flow of exudate removed from the wound site by the reduced pressure source using the secondary pressure source. The reduced pressure lumen or the secondary pressure lumen includes a skin contacting surface formed of a moisture permeable membrane comprising an air-impermeable film that allows moisture from the patient to transfer into the reduced pressure lumen or secondary pressure lumen through the moisture permeable membrane while maintaining reduced pressure at the wound site.

A free radical sterilization system having a chamber defining a region, and a generator for generating free radical reach effluent from a free radical electric generator and/or a vaporizer. A closed loop circulating system without a free-radical destroyer is provided for supplying the mixture of free radicals from the electric generator mixed with the hydrogen peroxide solution in the form of the effluent to the chamber. The free-radical sterilization system is used in sterilizing items in the chamber and, with an open-bottomed wound chamber, in treating wounds on a body.

A handpiece of a skin care device is disclosed. The handpiece includes a body part having an attaching and detaching hole provided on one side thereof, a solution introducing part linked with the attaching and detaching hole, an air discharging part, and a disposable tip module mounted onto the attaching and detaching hole of the body part. The tip module includes a cylinder body detachably mounted onto the attaching and detaching hole, and an inner cylinder configured to have a hollow inside and installed in the cylinder body. The hollow inside of the inner cylinder is linked with the solution introducing part and is configured as a solution injection flow channel in which a solution introduced from the solution introducing part flows when the tip module is mounted onto the attaching and detaching hole.

A fluid level indicator (50) for indicating the fluid level in an ophthalmic irrigation and/or aspiration system comprises a chamber (10) configured for holding a surgical fluid (F). The chamber (10) comprises at least one fluid port (72; 74) and a pressure port (71) for connection to a pressure source (20). A channel (140) extends from the chamber (10). The fluid level indicator (50) comprises a float (160) having a float body (162) disposed within the chamber (10) and a stem (164) extending from the float body (160) into the channel (10). The float body (160) is configured to move with the level of fluid within the chamber (10), thereby moving the stem (164) along the channel (140) extending from the chamber (10). The position of the stem (164) within the channel (40) indicates the fluid level within the chamber (10).

An apparatus for filling a wound can include an array of at least four truncated ellipsoids interconnected to define at least one fluid path through, for example perpendicular to, the array. The longest principal axis of each ellipsoid may be perpendicular to the array. Each truncated ellipsoid may be a spheroid and/or may include an approximately elliptical contact surface at each contact surface between two interconnected ellipsoids. Each fluid pathway may have four continuously-curved concave sides and may have a parallelogram-shaped cross-section with continuously-curved concave edges. A dressing may include the apparatus, a dressing layer coupled to the apparatus, a backing layer disposed over a surface of the dressing layer opposite the apparatus, and an attachment device disposed on at least a margin of the backing layer. Methods of treating various tissue sites using the apparatus or dressing with negative-pressure therapy are also disclosed.

A conduit includes a first end configured to be fluidly coupled to a wound site, and a second end configured to be fluidly coupled to a canister. The conduit additionally includes a central lumen extending between the first end and the second end. The conduit further includes a male interlocking member on a first side of the conduit and a female interlocking member on a second side of the conduit. Both the first side and the second side extend along a length of the conduit between the first end and the second end. The female interlocking member is configured to receive the male interlocking member.

A tube for a medical treatment system has a first channel for feeding an irrigation fluid from a console of the system to a medical treatment instrument of the system and a second channel for discharging an aspiration fluid from the instrument to the console. The first and the second channels are arranged in parallel. The first channel has a first wall and the second channel has a second wall. A second material of the second wall has a greater hardness than a first material of the first wall. The tube is formed from two individual tube elements for the channels. The tube elements are welded or adhesively bonded in a connection region. The difference between the hardness of the first material and the hardness of the second material is at least 10 ShA and at most 15 ShA.

To reduce the suffering of the patient and enable easier removal of excess fluid such as pleural effusion fluid from the chest space, the disclosure provides a catheter for chest drainage intended for removal of excess fluid from a chest space of a living body and to be placed in the living body in such a manner as to extend from an inside of the chest space to an outside of the living body. The catheter includes a passage member formed of a flexible sheet and having a passage through which the excess fluid is to be drained, and an indwelling member formed of an elastic body and provided at a proximal end of the passage member. The indwelling member has an inlet that allows the excess fluid to flow through. The indwelling member includes a retaining portion spreading in a flange shape and being retainable at a chest wall.