The present invention relates to a blood treatment cassette having a cassette body, embodied as a hard part, and a film, wherein the film is connected with the hard part and covers the hard part at least partially, wherein the hard part comprises at least one valve seat or valve section or one valve base of a valve, wherein the valve is embodied to take, in addition to a first, open position of the valve in which the valve base and the section of the film positioned above it do not touch each other, a second, closed position of the valve when applying force on the section of the film and wherein the valve base, in its longitudinal extension, comprises or is a non-straight section. The present invention also relates to a blood treatment apparatus connected with a blood treatment cassette.

A check valve, including a valve and a valve support surface, to permit a fluid to move through the check valve in a first direction and resist a fluid flow through the valve in a second direction, the valve having a valve diaphragm and an isolating bridge, with a portion of the valve engaging against valve support surface to resist deformation or stretching of the valve when a backflow of fluid into the check valve occurs. The valve support surface having a first support surface and a second support surface, and the valve positioned with the valve diaphragm spaced apart from the first support surface, and the isolating bridge spaced apart from the second support surface.

A catheter priming apparatus may include a barrier forming a reservoir. Fluid may be disposed within the reservoir. A support structure may be disposed within the barrier. The support structure may include an opening extending through the support structure and a connector configured to couple the catheter priming apparatus to a catheter system. A one-way valve may be coupled to the support structure and configured to allow the fluid to flow out of the reservoir through the connector in response to compression of a portion of the barrier aligned with the opening.

A wound care system for reduced pressure therapy comprising a covering device that can be fixed to the skin surrounding a wound and serving to produce a closed wound space containing the wound, a valve system, designed on the one hand to suck gases out of the wound space and on the other hand to counter the penetration of gases into the wound space, being assigned to the covering device after fixing the covering device to the skin surrounding the wound, the valve system being able to be coupled detachably to a suction device that can be operated to suck gases out of the wound space.

Disclosed is a fluid trap for use with, or comprising part of, a respiratory therapy system, d particular comprising part of, or configured to be connected to, a breathing limb, such as an expiratory limb, of a respiratory therapy system. The fluid trap comprises a container configured to contain fluid received from an inlet; a closure, the closure and container being configured to be removeably mounted together to close the container; and a valve configured to be removeably mounted on at least one of the container and the closure, and configured to be in a closed condition which prevents fluid from flowing through the inlet when the closure is not mounted on the container, the valve being further configured to be in an open position which allows fluid from the inlet into the container when the closure is mounted on the container.

An infusion set check valve assembly includes a self-contained housing that defines inlet ports and an outlet port. The assembly also includes at least one check valve disposed within the self-contained housing between the outlet channel and at least one of the inlet ports. The at least one check valve is configured to open for a first fluid to flow from a first inlet to a patient line via an outlet channel while a second fluid also flows from a second inlet to the patient line via the outlet channel. The at least one check valve closes to prevent the first fluid from flowing to the patient line via the outlet channel while the second fluid flows to the patient line.

The invention relates to an adjustable implantable throttle for controlling a drainage rate in implantable drains for cerebrospinal fluid drainage. Despite the existence of proven valves, the invention has set itself the object of improving valves. It solves this by making at least one effective length of at least one channel adjustable.

A valve assembly for a dental suction system. The valve assembly includes a valve body having an inlet, an outlet and a fluid flow path extending between the inlet and the outlet. The valve assembly also includes a valve plug positioned at least partially within the valve body and including a through-passage. The valve plug is rotatable relative to the valve body to selectively alter a flow of fluid along the fluid flow path. The fluid flow path exhibits a varied cross-sectional area along a length of the fluid flow path.

Fluid connector systems including first and second connector portions couplable together to form a fluid pathway therethrough, and can resist fluid flow through the connector when the connector portions are separated from each other. A connector portion can include a connector housing, a luer portion, and a deformable valve member. The deformable valve member is disposed within the connector housing and includes a spherical portion extending partially through a valve opening of the connector housing. The spherical portion defines a slit, and the deformable valve member is configured to selectively prevent fluid flow from the housing volume through the valve opening and to deform to expand the slit and permit fluid flow from the housing volume through the valve opening.

Valve components positioned in fluid connector assemblies, including universal fluid connector assemblies, are shown. A valve component is designed to open or close based on fluid pressure from a medical fluid applied to the valve component. Normally, when no force is acting on the valve component, the valve component is in an open position and portions of the valve components are spaced apart by a threshold force, thus forming a valve chamber. However, in an exemplary embodiment, when an applied force by the medical fluid is at least at the threshold force, the portions of the valve component contact each other and the valve component transitions to a closed position, thereby preventing the medical fluid from passing through the valve component, and accordingly, preventing the medical fluid from passing through the fluid connector assembly.