A device that helps clear a fluid or other material lodged in a person's throat has a barrel with an open proximal end and an opening laden distal end. A plunger is slidably disposed within the barrel such that the plunger, by being manually drawn outwardly, creates suction within the barrel drawing air through the opening. A single or multi-section tube, flexible on at least its distal end, is fluid flow connected to the opening and has a face mask along its length. The distal end of the tube is intubated with a person proximate the fluid or other material so that as the plunger is drawn outwardly through the barrel, the suction created within the barrel causes air to be drawing in through the tube and into the barrel thereby helping draw out and dislodge the fluid or other material. A backflow valve located on the barrel helps clear the barrel of such things as vomit that might have been drawn into the barrel.

A cap for intake and delivery of a fluid from a syringe is described. The cap includes an outer cap assembly comprising a fluid inlet path and a fluid outlet path and an inner cap assembly configured for innertion into a fluid nozzle of the syringe and to provide selective fluid communication between an interior of a syringe and the fluid inlet path or the fluid outlet path. The outer cap assembly is slidable relative to the inner cap assembly between a first filling position, where the interior of the syringe is in fluid communication with the fluid inlet path, and a second delivery position, where the interior of the syringe is in fluid communication with the fluid outlet path. The outer cap may further slide, relative to the inner cap assembly, to a third closed position where the interior of the syringe is fluidly isolated from the fluid inlet path and the fluid outlet path. Syringes including the cap are also described.

A check valve may include an upper housing defining an inlet, a lower housing defining an outlet, and a cavity interposed between and defined by the upper and lower housings for fluidly connecting the inlet and the outlet. The check valve may further include a flexible valve member mounted in the cavity to selectively permit fluid flow in a first direction, and prevent fluid backflow in a second direction opposite to the first direction. A filter member may be mounted in the upper housing, upstream of the flexible valve member. The filter member may have an elongated portion configured to maximize surface area thereof exposed to the fluid flow, and restrict passage of undesirable matter in fluid flowing through the check valve.

The present invention provides a microjet drug injection device equipped with a backflow prevention valve, the microjet drug injection device comprising an upper housing, a lower housing, a compartment, and a backflow prevention valve.

A connector-with-integrated-check-valve for minimizing microbial migration to catheter-tubing is formed from three parts: a connector-for-catheter-tubing that is hollow and with an internal valve seat; an elastomer disc shaped gate; and a connector-for-extension-tubing that is hollow and with support-surfaces. When one end of the connector-for-catheter-tubing is attached to one end of the connector-for-extension-tubing, a pocket is formed where the seat is disposed opposite and facing the support-surfaces; the gate is disposed within this pocket; such that when the gate contacts this seat due to urine backflow (reflux), the connector-with-integrated-check-valve is closed to such urine backflow; and where a remaining end of the connector-for-catheter-tubing is attachable to catheter-tubing; and where a remaining end of the connector-for-extension-tubing is attachable to the extension-tubing, such that there is a continuous urine flow path from the catheter-tubing, to the connector-with-integrated-check-valve when open, and to the extension-tubing.

A cannula for the circulation of a fluid in an artery, includes a main lumen conveying a volume of fluid towards a first distal end; an accessory lumen including at least one inner portion arranged inside the main lumen, including: a proximal end situated downstream from the proximal end of the main lumen so as to capture a fraction of the flow of fluid entering the main lumen; a bent portion modifying the direction of flow of the fluid flow captured by the accessory lumen with respect to the direction of flow of the fluid emerging from the first end; a second distal end situated upstream from the first distal end of the main lumen, emerging on a side opening of the cannula so as to direct the captured fraction of liquid in the modified direction of flow.

A chemical liquid injector that can easily set various injection conditions according to a region and an objective to be imaged. The chemical liquid injector includes two piston driving mechanisms for operating syringes filled with a first chemical liquid and a second chemical liquid, respectively, an input unit for receiving an input of a data, and an injection control unit for controlling an operation of the piston driving mechanisms. The injection control unit is set with a multistage injection mode in which injection operations are performed in a plurality of injection phases. In the multistage injection mode, the injection control unit is configured to receive the input of the mixing rate of the first chemical liquid and the second chemical liquid for each of the plurality of injection phases, set injection conditions of the first chemical liquid and the second chemical liquid so that the first chemical liquid and the second chemical liquid are injected at the received mixing rate, and control the operation of the driving mechanisms according to the set injection condition.

This device is used to clear clots and blockages from chest drainage tubes. This invention relates to patient safety after open-heart surgical procedures, wherein postoperative drainage from the surgical site is a critical component of care. Blocked drainage tubes can cause dangerous retained blood complications, most notably, cardiac tamponade, which essentially smothers the heart.

A hydraulically actuated valve device includes a valve body having an inner cavity, an inlet channel extending to the inner cavity, an outlet channel extending from the inner cavity, and an open end that opens to the inner cavity. A septum is located in the inner cavity to seal the open end of the valve body and to receive a needle through which an operating fluid may be selectively injected into or withdrawn from the inner cavity to increase or reduce a fluid pressure in the inner cavity. A valve closing member has an unactuated state to enable a first fluid to flow from the inlet channel to the outlet channel when the fluid pressure of operating fluid in the inner cavity of the valve body is below a closing pressure, and inhibits the first fluid from flowing out of the inner cavity through the outlet channel when the operating fluid in the inner cavity of the valve body is at or above the closing pressure.

A check valve includes an upper housing defining an inlet of the check valve, a lower housing defining an outlet of the check valve, and a cavity interposed between and defined by the upper and lower housings for fluidly connecting the inlet and the outlet. The check valve further includes a valve member mounted in the cavity to selectively permit fluid flow in a first direction, and prevent fluid backflow in a second direction opposite to the first direction. The valve member includes a valve body and a valve stem portion extending axially through a central axis of the valve body. The valve member may further include a plurality of feet disposed about and extending longitudinally from an outer circumferential perimeter of the valve body.