A valved container assembly which has a container for containing a fluid, the container extending in an axial direction and having an open front end and a valve disposed in the container. The valved container assembly is configured so that forward axial movement of the valve relative to the container is inhibited. A plunger element is disposed axially rearward of the valve and is axially moveable in the container. The plunger element is configured to increase the pressure of a fluid in a first volume of the container upon forward axial movement relative to the valve. The valve includes a channel bypassing the permanent seal, the channel having a first opening in fluid communication with the atmosphere outside of the valved container assembly and a second opening selectively sealed from the first volume by a resilient seal.

A bi-directional valve assembly, including valves for use in closed-ended catheters or other elongate tubular devices, is disclosed. In one embodiment, a catheter assembly for insertion into a body of a patient is disclosed and comprises an elongate catheter tube including an outer wall that at least partially defines at least one lumen that extends between a proximal end and a closed distal end thereof. The catheter tube includes a valve assembly that in turn includes a linear slit valve defined through the outer wall of a distal segment of the catheter tube, and a deformation region. The deformation region includes a compliant segment disposed in the outer wall of the catheter tube and a thinned portion of the outer wall. The compliant segment and thinned portion of the deformation region cooperate to preferentially deform the outer wall and open the slit valve during aspiration through the catheter tube.

In one aspect, a valve includes a valve body rotatable about a central axis of the valve body, an interior channel adjacent the valve body for permitting a fluid to flow through an axial opening of the interior channel, and a plug within the interior channel that is movable between a first axial position at the axial opening and a second axial position spaced apart from the axial opening. In the first axial position, the plug closes the axial opening to prevent the fluid from flowing through the axial opening in a first direction and to prevent the fluid from flowing through the axial opening in a second direction that is opposite to the first direction. In the second axial position, the plug permits the fluid to flow through the axial opening into the interior channel in the first direction.

A fluidic group (21) couplable to a first container (24) adapted to contain a drug and a second container (22) adapted to contain an ingredient, comprising: a syringe (154) comprising a movable piston (150) defining a chamber (162a) having a variable volume; a first (171, 172) and a second (25) coupling group selectively fixable to the second (22) and, respectively, to the first (24) container; a forking element (166) having a first (166′), a second (166″) and a third (166′″) inlet in fluid communication with each other and, respectively, with the first coupling group (171, 172), with the second coupling group (25) and with the chamber (162a); a first one-way valve (168) interposed between the first coupling group (171, 172) and the forking element (166) and controllable to allow the passage of the ingredient from the second container (22) to the chamber (162a); and a second one-way valve (176) interposed between the second coupling group (25) and the forking element (166) and controllable to allow the passage of the ingredient from the chamber (162a) to the first container (24).

Check valve assemblies for fluid flow sets and devices are provided. The check valve assembly includes an inlet body including a fluid inlet, first and second seal beads, and a central channel. An outlet body includes a fluid outlet and a stem having a centering post, the centering post received by the central channel of the inlet body. A seal includes inner and outer rings, wherein the inner ring is configured to engage with the first seal bead and the outer ring is configured to engage with the second seal bead in a fully sealed position of the check valve assembly. Fluid flow sets and methods for manufacturing check valve assemblies are also provided.

A syringe is provided having a hub with an orifice, first and second barrels having interior surfaces to form respective lumens, a slider, and an optional test indicator. The first and second barrels slideably receive respective first and second plungers for movement therein. The slider is operable to provide a fluidly communicative path between the orifice of the hub and the first and second barrel lumens. The optional test indicator is responsive to at least one characteristic of bodily fluid, the test indicator positioned to be exposed to any bodily fluid drawn into the first barrel lumen and visible from an exterior of the first barrel.

A pump generates a vacuum at a wound site via first tubing. A negative pressure circuit is defined by a canister, the first tubing and the wound site. A controller of a therapy device operates the pump to apply a first negative pressure to the entirety of the negative pressure circuit, following which ambient air is allowed to flow into the negative pressure circuit. The controller also operates the pump to apply a second negative pressure to a selected portion of the negative pressure circuit exclusive of the wound site, following which ambient air is allowed to flow into the selected portion. A quantity of fluid to be delivered to the wound site via a second tubing is determined by comparing measured parameters related to the flow of air into the negative pressure circuit to parameters measured with respect to the flow of air into the selected portion.

A fluid control device includes a piezoelectric pump, an inhaler, and a valve. The piezoelectric pump has a gas suction hole and a gas discharge hole. The inhaler has a container, an inhalation port, and a connection hole. The valve has a first ventilation hole, a second ventilation hole, a third ventilation hole, a first valve housing, a second valve housing, and a valve body. The first ventilation hole of the valve is connected to the connection hole of the inhaler. The second ventilation hole of the valve is connected to the suction hole of the piezoelectric pump. The third ventilation hole of the valve is opened to the atmosphere. The valve body is held between the first valve housing and the second valve housing, and configures a first region and a second region.

A valve device for a medical fluid line system includes a main body, the main body having a first fluid passage and a second fluid passage, each fluid passage of the first and second fluid passages extending between an inlet side and an outlet side of the main body. The main body has a first wall portion and a second wall portion which are each elastically displaceable, under an effect of fluid pressure, relative to a substantially dimensionally stable web portion of the main body. Each wall portion of the first and second wall portions is arranged on the web portion, forming one of the first and second fluid passages, in such a way that the first fluid passage is substantially uninfluenced by a fluid-pressure-induced deformation of the second wall portion, and the second fluid passage is substantially uninfluenced by a fluid-pressure-induced deformation of the first wall portion.

A leak control system (26) for an evacuation system (12) of an insufflation system (1), for controlling leakage of insufflating gas from a vessel (5) of a subject being insufflated. An evacuation conduit (20) connects a Venturi vacuum creating device (14) to the vessel (5) through a pressure relief valve (27) operable from a closed state to an open state in response to a pressure drop across the pressure relief valve (27) in the direction of the arrow A exceeding a predefined pressure drop value. The vacuum creating device (14) is operable in response to a signal from a pressure sensor (10) detecting pressure in the cavity (5) exceeding a predefined pressure value for applying a vacuum to the evacuating conduit (20) to increase the pressure drop across the pressure relief valve (27) to the predefined pressure drop value, for in turn operating the pressure relief valve (27) into the open state. On the pressure in the vessel (5) being reduced below the predefined pressure value, the vacuum creating device (14) is deactivated, and the pressure relief valve (27) transitions into the closed state, thereby preventing further leakage of insufflating gas though the Venturi vacuum creating device (14).