A device for delivering an agent may comprise a source of agent; a mixing chamber for receiving fluid and the agent; an outlet in fluid communication with the mixing chamber to deliver the fluid and the agent; and an actuator configured to (1) deliver a first flow of the fluid substantially free from the agent through the outlet; (2) after delivering the first flow, deliver a second flow of the fluid and the agent through the outlet; and (3) after delivering the second flow, deliver a third flow of the fluid substantially free from the agent through the outlet.

The invention relates to a blocking and/or restricting valve having a valve housing which has a fluid system having a fluid inlet, a fluid outlet and a fluid chamber arranged therebetween, wherein the fluid chamber comprises a blocking geometry and is bounded by a barrier membrane with respect to the blocking geometry, wherein the barrier membrane is connected to a tappet on its side remote from the fluid chamber (8) such that it can be pressed toward the blocking geometry by a movement of the tappet and can be lifted thereby, and wherein the tappet is arranged in a freely floating manner in a hollow space of the valve housing.

A method for treating pleural effusion in a patient, the method comprising: providing a valve comprising: a body having a distal end, a proximal end and a lumen extending therebetween; an inlet disposed at the proximal end of the body, the inlet being fluidically connected to the lumen; an outlet disposed at the distal end of the body, the outlet being fluidically connected to the lumen; and at least one valve element disposed in the lumen of the body, the at least one valve element being a one-way valve element configured to permit the passage of fluid in a single direction through the lumen of the body; and implanting the valve in the body of the patient such that the inlet of the valve is fluidically connected to the pleural cavity of the patient, and such that the outlet of the valve is fluidically connected to a second body cavity.

An anesthetic tank includes an insertion mouth for inserting an injection adapter of an anesthetic container, and a storage portion communicating with the insertion mouth. A volatile anesthetic inside of the anesthetic container is injected into the storage portion. An identifying member is arranged on the outside of the insertion mouth and is rotatable around the center axis of the insertion mouth. The identifying member has key groove formed in the internal surface of an insertion hole for inserting the injection adapter. The key groove are used for identifying the type of the volatile anesthetic in collaboration with keys formed in the injection adapter. A cover member has an opening formed in the position facing the insertion mouth and the insertion hole and presses the peripheral part of the identifying member.

An anesthetic tank includes an insertion mouth for inserting an injection adapter of an anesthetic container, and a storage portion communicating with the insertion mouth. A volatile anesthetic inside of the anesthetic container is injected into the storage portion. An identifying member is arranged on the outside of the insertion mouth and is rotatable around the center axis of the insertion mouth. The identifying member has key groove formed in the internal surface of an insertion hole for inserting the injection adapter. The key groove are used for identifying the type of the volatile anesthetic in collaboration with keys formed in the injection adapter. A cover member has an opening formed in the position facing the insertion mouth and the insertion hole and presses the peripheral part of the identifying member.

A suction/irrigation medical device valve system comprises a first valve plunger configured for insertion into a first valve plunger channel. The first valve plunger has a first latch member disposed at a distal end with a first sealing member and a first valve opening disposed proximally from the first latch member. The system also comprises a second valve plunger configured for insertion into a second valve plunger channel. The second valve plunger includes a second valve opening that is longer than the first valve opening. The system also comprises a valve body having the first and second valve plunger channels. The first and second valve plunger channels are configured to receive the first and second valve plungers, respectively.

A device for delivering an agent may comprise a source of agent; a mixing chamber for receiving fluid and the agent; an outlet in fluid communication with the mixing chamber to deliver the fluid and the agent; and an actuator configured to (1) deliver a first flow of the fluid substantially free from the agent through the outlet; (2) after delivering the first flow, deliver a second flow of the fluid and the agent through the outlet; and (3) after delivering the second flow, deliver a third flow of the fluid substantially free from the agent through the outlet.

When employing a valve in a medical device in or near a bore of a magnetic resonance (MR) scanner, MR-compatible materials are employed to minimize the susceptibility of the valve to the strong magnetic fields generated by the MR scanner. An MR-compatible actuator comprises a shame memory alloy (SMA) wire or member (12) that is actuated by application of a constant power signal. The constant power signal is supplied by a control circuit (50) that is generated using a power feedback signal derived from measured current and voltage feedback signals. Once the SMA member is actuated, the power signal can be reduced and pulse width modulated to maintain the SMA member in an active state, which in turn maintains the valve in a closed state until the power signal is terminated.

One embodiment is directed to a system for injecting, comprising a syringe body defining an interior medicine chamber; a stopper member configured to be inserted into the interior medicine chamber to contain medicine within the medicine chamber; a plunger member configured to be manually manipulated to insert the stopper member relative to the syringe body; and a needle having proximal and distal ends, the proximal end comprising an anchoring geometry configured to be at least partially inserted into the stopper member such that upon retraction of the stopper member, the needle is pulled proximally along with the stopper to be at least partially contained within the interior medicine chamber.

A flow selector valve assembly for an enteral feeding pump system (i.e., an enteral feeding pump system including a fluid delivery set with first and second feeding tubes, an enteral feeding pump and a pinching mechanism for regulating the flow of nutrient formula or water out of the first and second feeding tubes), and a twin port adapter for use in the valve assembly. The twin port adapter includes a body configured to receive the first and second feeding tubes therein, and a feeding tube guide rotatably connected to the body and configured to secure the first and second feeding tubes within the body.