The present invention relates to an expression kit (1) for extraction of breast milk from a female breast, comprising a funnel (2) for receiving the breast therein, a housing (4), a container (5) for receiving the breast milk, a connection port (7) for connection to a vacuum source, and a membrane element (6) arranged in the housing (4) between the funnel (2) and the container (5) for sealing the funnel (2) with respect to the connection port (7), the funnel (2) with respect to the housing (4) and the housing (4) with respect to the container (5).

A male reflux valve comprising a distal body portion and a proximal body portion, the proximal body portion having a male connection for connection to a female connection of an access device, a valve element operatively positioned within the distal body portion, a core operatively positioned within the distal body portion to retain the valve element into sealing engagement with the distal body portion and an actuator reciprocably retained within a generally circular cylindrical longitudinal bore of the proximal body portion in engagement with the valve element to open the valve element when engaged by the female connection of the access device.

A multi-use intravenous infusion assembly is presented which includes a septum actuator having various features to prevent over-insertion of the septum actuator through a slit in a blood control septum. By preventing over-insertion of the septum actuator, the slit of the septum is able to repeatedly self-close following removal of an external Luer device. Thus, the intravenous infusion assembly may be used repeatedly without exposing a clinician to blood and other infusion fluids.

A valve (1, 11, 19) for an inhalation device comprising an interior volume that is delimited at least partially by a valve wall (4, 17, 21), a permanent opening (29) as well as a valve functional area (6), whereby the valve functional area (6) is configured to be at least almost closed below an opening pressure difference and to be open above an opening pressure difference such that above the opening pressure difference, a fluid can flow through the permanent opening (29) into the interior volume and out of the valve functional area (6), the valve comprising an inversion protector that is configured to impede or prevent inversion of the valve wall (4, 17, 21).

An anti-free-flow valve includes a tube and a membrane. The tube extends from a first end of the tube to a second end of the tube. The tube defines a hollow cavity. The membrane is attached to an interior surface of the tube and extends across the hollow cavity to obstruct fluid flow through the hollow cavity. The membrane is spaced apart from the first and second ends of the tube. The membrane defines a slit therethrough that is configured to transition from a closed state that restricts fluid flow to an open state that permits fluid flow through the slit responsive to compression or expansion of the tube proximate to the membrane.

A kit of parts includes a urological device and a catheter. The urological device has a stem defining a lumen, a valve connected to a proximal portion of the stem and located in the lumen, and a head part connected to the stem and extending radially around the valve. The catheter is adapted to insert the urological device into a urethra of a user.

A catheter insertion system includes a housing extending along a longitudinal axis. A needle extends distally from a distal end of the housing. The needle has a longitudinal passage coaxially aligned with the housing. A catheter has a length and is sized and shaped to be advanced from a retracted position within the longitudinal passage of the needle to an extended position with at least a portion of the catheter length extending beyond a distal tip of the needle. The needle is typically configured to be retracted back into the housing after the catheter has been advanced, thus providing an integrated catheter and catheter insertion apparatus. After needle retraction, the housing may be taped to the patient's skin while the needle remains protected within the housing. A luer on the catheter may then be connected to a fluid or other source in an otherwise conventional manner.

The intravenous catheter device (100) includes a catheter hub (102), a valve member (158), an actuator member (176) and a valve closure member (192). The valve member (158) includes a convex portion (162) provided with slits (170) defining prongs (172). The slits (170) are configured to open when a needle (116) is pierced through the slit (170) to puncture a vein of a patient. The valve closure member (192) is disposed inside the catheter hub (102) such that the first surface (194) of the valve closure member (192) abuts the convex portion (162) of the valve member (158). When the luer lock member (206) abutting the actuator member (176) inside the catheter hub (102) is disengaged, the valve closure member (192) is adapted to push the prongs (172), closing the passage (204) for the fluid flow and preventing blood flow from the punctured vein of the patient.

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 surface portion and a second surface portion, and the valve positioned with the valve diaphragm spaced apart from the first surface portion, and the isolating bridge spaced apart from the second surface portion.

A medical connector includes: a first connection section that defines a first passage; a second connection section that defines a second passage communicating with the first passage; and a rotation control section that controls relative rotation of the first and second connection sections. The second connection section includes a first wall face configured to abut on the first connection section to restrict the first connection section from moving in a direction to be separated from the second connection section. In a state in which the first wall face abuts on the first connection section, the rotation control section allows the second connection section to rotate relative to the first connection section in a first circumferential direction about the axis and restricts the second connection section from rotating relative to the first connection section in a second circumferential direction opposite to the first circumferential direction.