Embodiments disclosed herein are directed to a connector for a fluid drainage having a body defining a drainage lumen extending longitudinally from a distal portion to a proximal portion. The body can include a piston housing and an inlet in fluid communication with a positive air pressure source. A piston is slidably engaged with the piston housing along a transverse axis between a first position and a second position. In the first position, the piston provides fluid communication between the distal portion and the proximal portion of the drainage lumen and occludes fluid communication between the inlet and the drainage lumen. The piston in the second position occludes fluid communication between the distal portion and the proximal portion of the drainage lumen and provides fluid communication between the inlet and the drainage lumen to clear dependent loops, while preventing distal fluid flow into a catheter.

A suction/irrigation medical device comprises a valve body having one or more conduits fluidically coupled thereto and a first channel extending through the valve body. The medical device also comprises a first valve plunger disposed along the first channel and configured to move along an axis to open and close the first channel. The first valve plunger has a first opening to permit a fluid to flow through the first channel. The medical device also comprises a second valve plunger disposed along the first channel and along a second channel to couple the second channel into the first channel when the second valve plunger is in a first position. The second valve plunger has a second opening that has at least one dimension that is greater than a corresponding dimension of the first opening of the first valve plunger.

The invention relates to a pneumatic manifold for controlling a fluid level in an arterial and/or venous drip chamber of a dialysis system. The pneumatic manifold includes pneumatic valves fluidly connected to conduits and one or more pumps. Selectively activating the pneumatic valves can result in pressure changes for raising or lowering a fluid level in the arterial and/or venous drip chambers.

A bi-stable popper valve and a device for detecting blockage in a flow of a fluid are provided. The valve includes a membrane supporting two conformations: in a first conformation the membrane is convex in relation the upstream fluid, and in a second conformation the membrane can be concave in relation to the upstream fluid, such that in the first conformation the flow of the fluid through the membrane is prevented and in the second conformation the flow of the fluid through the membrane is permitted through a pore defined by the membrane in only the second conformation. The membrane changes from the first conformation to the second responsive to a pressure of the fluid meeting or exceeding an opening pressure value of the membrane. A sensor can detect a shift from the first conformation to the second conformation, indicating a flow, or absence of flow, of the fluid.

A system and method for providing fluid to a tissue site is described. The method fluidly couples an instillation therapy system to the tissue site and monitors a pressure supplied to the tissue site by a reduced-pressure source with the instillation therapy system for a time period. The method provides fluid to the tissue site with the instillation therapy system in response to the pressure at the tissue site during the time period. The system includes a pressure sensor fluidly coupled to the tissue site to measure a pressure proximate the tissue site. A valve and a flow meter are fluidly between a fluid reservoir and the tissue site. A controller is communicatively coupled to the pressure sensor and the valve and configured to monitor the pressure at the tissue site and a volume of fluid flow to the tissue and, in response, operate the valve.

Systems, methods, and apparatuses for irrigating a tissue site are described. The system can include a tissue interface and a sealing member configured to be placed over the tissue site to form a sealed space, and a negative-pressure source fluidly coupled to the sealed space. The system includes an irrigation valve having a housing, a piston disposed in the housing, a fluid inlet to fluidly couple a fluid inlet chamber to a fluid source, and a fluid outlet to fluidly couple a fluid outlet chamber to the sealed space. A piston passage extends through the piston and fluidly couples the fluid inlet chamber and the fluid outlet chamber, and a biasing member is coupled to the piston to bias the irrigation valve to a closed position. The negative-pressure source is configured to move the piston between the closed position and an open position to draw fluid to the sealed space.

Fluid flow manifold assemblies for use in fluid flow sets are provided. The fluid flow manifold assembly includes a body having a main fluid channel and a reinforcing plate, the main fluid channel having a fluid inlet, a fluid outlet and a drug port. A flow control assembly is disposed opposite the main fluid channel from the drug port. The flow control assembly is configured to shut off fluid flow through the drug port into the main fluid channel with a plunger of the flow control assembly in a closed position and to allow incremental levels of fluid flow through the drug port into the main fluid channel by variably retracting the plunger based on rotation of a knob of the flow control assembly.

A device and a method for delivering a flowable ingestible medicament into the gastrointestinal tract of a user. The device includes a vibrating ingestible capsule attached to a medicament delivery compartment. The medicament delivery compartment includes a housing including a portal, a medicament reservoir, a reservoir biasing mechanism applying pressure to the reservoir, a resilient conduit extending from the reservoir to the portal, and a valve including a weight and a spring adapted, when closed, to bias the weight against the conduit so as to block flow therethrough, and, when open, to remove the weight from the conduit to allow fluid to flow through the conduit. When the vibrating agitator is in the vibration mode of operation, vibrations exerted thereby are applied to the valve biasing mechanism and periodically transition the valve between the closed operative orientation and the open operative orientation.

Systems and methods for directing fluid flow are described. In some embodiments, a system may include a first port, a second port, and a third port. The system may have a first state in which a male fitting of a device is not inserted in a female fitting of the third port. The valve assembly may block a first fluid path defined between the first port and the third port when the system is in the first state. The system may also have a second state in which a male fitting of a device is fully inserted in the female fitting of the third port. The valve assembly may block a second fluid path defined between the first port and the second port when the system is in the second state.

An enteral feeding valve assembly includes a housing assembly that is fluidly coupled with an upstream line and a downstream line. A diverging conduit inwardly extends from an inlet and a primary conduit inwardly extends from an outlet of the housing. The diverging conduit splits into a bypass conduit and a flow-through conduit. The flow-through conduit is fluidly coupled with the primary conduit by a check valve. A plunger valve includes one or more plunger conduits and moves in a first direction to fluidly couple the inlet with the primary conduit and the outlet via the bypass conduit and the one or more plunger conduits. The plunger valve moves in a second direction to de-couple the inlet from the primary conduit and the outlet via the bypass conduit and the one or more plunger conduits. The flow-through conduit directs the fluid to the outlet through the check valve.