A connector for forming a fluid flow pathway by connection with a reciprocal connector. Both the connector and reciprocal connector include a fluid flow blockage partsheathed within an axially compressible sheath part. A first bearing surface receives an urging force to retract the blockage part axially along the sheath part. A terminal end of the sheath part defines a second bearing surface containing a fluid flow opening with the fluid flow blockage part retractably therein. A first chassis part includes a first catch part. A second chassis part includes a second catch part and a third bearing surface spaced from the second catch part along the second chassis part. Retraction of the blockage part forms a fluid flow pathway not sooner than immediately when the openings meet to allow fluid transfer the openings avoiding fluid leakage between connected connectors.

A system for priming an infusion pump is disclosed. The system includes a priming cap including a septum and configured to matably connect with a male part comprising a needle and attached to a length of tubing for fluid, wherein when matably connected with the male part, the priming cap occludes the tubing.

A system for priming an infusion pump is disclosed. The system includes a priming cap including a septum and configured to matably connect with a male part comprising a needle and attached to a length of tubing for fluid, wherein when matably connected with the male part, the priming cap occludes the tubing.

A method of manufacturing tubing suitable for use as a component of a medical device, such as a catheter body, and the real-time adjustment of characteristics of the tubing as it passes from one reel to another reel during manufacture. Thus, a length of tubing is manufactured that includes a plurality of segments of different flexibilities and the length of tubing is then cut into a plurality of sub-lengths of tubing that are suitable for use as a component of a medical device. In one embodiment, a method of manufacturing a length of catheter tubing comprises: extruding a base layer; overlaying a braided layer on the base layer; overlaying a sub-jacket layer over the braided layer; overlaying an outer jacket on the jacket sub-layer; and heating at least a portion the jacket sub-layer to change a characteristic of the length of catheter tubing.

Medical devices are provided comprising a spike including proximal and distal ends, and a central axis extending from the proximal to the distal end; a valve body; a biasing body which biases the valve body; a distal tube that moves integrally with the valve body to both sides in the axial direction relative to the spike; a proximal tube fixed in the axial direction relative to the spike, the distal tube comprising a guided portion guided toward the proximal tube, and an engagement control unit which moves the guided portion toward one side in the radial direction by connection of the different medical device to the distal tube allowing the guided portion to engage with the proximal tube, and moves the guided portion toward the other side in the radial direction releasing engagement with the proximal tube when the different medical device is detached from the distal tube.

The invention is directed to an connector comprising a first part and a second part, each provided with a contact surface and at least one non-contact surface facing away from the contact surface, at least one opening in the contact surface having an fluid connection to at least one opening of the non-contact surface, a releasable covering of the opening in the contact surface, and complementary means for mechanically coupling the parts at the contact surfaces to form the connector. The complementary means for mechanically coupling the parts are configured to mechanically interlock with each other.

The invention is directed to an connector comprising a first part and a second part, each provided with a contact surface and at least one non-contact surface facing away from the contact surface, at least one opening in the contact surface having an fluid connection to at least one opening of the non-contact surface, a releasable covering of the opening in the contact surface, and complementary means for mechanically coupling the parts at the contact surfaces to form the connector. The complementary means for mechanically coupling the parts are configured to mechanically interlock with each other.

A protective membrane for a medical luer connector may include a cover having an upper surface, a lower surface having a mating portion for coupling to a mating surface of the medical luer connector, and an outer perimetal surface. The protective membrane may further include a flexible pull tab extending from the outer perimetal surface of the cover, and an adhesive overlaying the mating portion of the lower surface for adhering to the mating surface of the medical luer connector.

A protective membrane for a medical luer connector may include a cover having an upper surface, a lower surface having a mating portion for coupling to a mating surface of the medical luer connector, and an outer perimetal surface. The protective membrane may further include a flexible pull tab extending from the outer perimetal surface of the cover, and an adhesive overlaying the mating portion of the lower surface for adhering to the mating surface of the medical luer connector.

A drug delivery system for injecting a medicament may include a housing defining a cavity, a container received within the cavity and configured to receive a medicament with the container including a closure, a valve assembly received within the cavity and including a piercing member configured to pierce the closure of the container, and a connector arrangement provided between the container and the valve assembly, the connector arrangement movable between a first, pre-use position maintaining sterility between the closure of the container and the valve assembly and a second, use position permitting fluid communication between the container and the valve assembly.