A fluid transfer device such as a syringe may include a fluid chamber in communication with a male connector tip. The male connector tip is tapered to form a friction fit when inserted in a corresponding female hub. A disconnecting member, e.g., in the form of a lever member has a front surface moveable along the male connector tip between a first position proximal to the fluid chamber and a second position spaced from the first position towards a distal end of the male connector tip so as to release the friction fit. A catch is arranged to catch the female hub after it has been released from the friction fit by the lever member moving towards the second position. The catch may be released when the lever member pivots back towards the first position under the resilient bias of a spring tongue.

In one aspect of the invention, a needle assembly is provided, including: a body having a proximal end, a distal end, and a channel located therebetween, the body being configured to be mounted to an injector; a needle fixed to the body, the needle having proximal and distal ends, the distal end extending distally from the distal end of the body and being formed for insertion into a patient, the proximal end of the needle being in communication with the channel; and, a filter disposed in the channel proximally of the proximal end of the needle. Advantageously, a needle assembly is provided which permits mixing of at least two substances in preparation for injection, without modification to the associated injector.

A pen needle, comprising a reusable adapter configured for attachment to a distal end of a medication pen, the adapter having a proximal needle for accessing the interior of the pen injector and a fitting on the distal side for mating with a patient end needle assembly, and a disposable patient-end needle assembly having a base configured for mating with the fitting on the distal side of the adapter and a patient-end needle extending from a distal end of the base.

Junction assemblies for joining intravenous (IV) devices to tubing are provided. A junction assembly includes a component connector and a shaped memory polymer (SMP) member formed of a shape changing material. The junction assembly allows movement of the tube along the component connector when the SMP member is in an expanded state and the junction assembly retains the tube securely against the component connector when the SMP member is in a contracted state. The shape changing material changes to one of the expanded state and the contracted state upon being subjected to an external stimuli. Methods of assembling junction assemblies are also provided.

Described is a medical adapter assembly comprising an end including a neuraxial fitting that is not directly connectable to a standard luer fitting, an opposing end including a fitting connectable to an intravenous medical device, and a check valve that allows fluid flow from the end with the standard luer fitting to the end with the neuraxial fitting, but prevents fluid flow from the end with the neuraxial fitting to the end with the standard luer fitting. Methods of using the medical adapter assembly and kits containing the medical adapter assembly are also described.

Junction assemblies for joining intravenous (IV) devices to tubing are provided. A junction assembly includes a component connector and a shaped memory polymer (SMP) member formed of a shape changing material. The junction assembly allows movement of the tube along the component connector when the SMP member is in an expanded state and the junction assembly retains the tube securely against the component connector when the SMP member is in a contracted state. The shape changing material changes to one of the expanded state and the contracted state upon being subjected to an external stimuli. Methods of assembling junction assemblies are also provided.

A hard-packaged safety needle device comprises a needle hub comprising a distal portion and a proximal portion, a needle cannula extending from the distal portion of the needle hub, and a hard needle enclosure comprising a needle cover, an adapter and a cap. The needle cover is configured to house the needle cannula, and the adapter has a tapered aperture configured to create an interference fit and a sterility barrier with the tapered outer surface of the needle cover. The caps includes a distal opening defining a first cavity, the cap being configured to interdigitate with the adapter by the first cavity of the cap receiving a proximal portion of the adapter.

A needle-equipped outer tube includes a needle; a joint member that supports the needle, the needle being insert molded or thermally welded to the joint member; and an outer tube including a connection section, wherein the joint member is thermally welded to the connection section of the outer tube.

Some embodiments are directed to a needle assembly that includes a needle having a textured portion and non-textured portion adjacent to the textured portion, and a hub arranged over at least a part of the textured portion of the needle. The textured portion includes laser etched grooves formed on an outer surface of the needle and oriented in a circumferential direction of the needle. Each of the laser etched grooves has two protruded portions and a dented portion interposed between the two protruded portions. Each of the two protruded portions has a top surface located above an outer surface of non-textured portion, and the dented portion has a bottom surface located below the outer surface of non-textured portion.

Safe insulin needle assembly includes protection sheath, needle, safety protection sleeve, pressure seat and needle holder. The needle is arranged on the central axis of the needle holder. The pressure seat is sheathed over the upper portion of the needle holder. The safety protection sleeve is sheathed on the needle holder and the pressure seat as a whole. The upper protection of the safety protection sleeve is connected to and cooperates with the pressure seat. The needle protrudes out of the top end of the upper portion of the safety protection sleeve. The lower portion of the safety protection sleeve is connected to and cooperates with the lower portion of the needle holder. The protection sheath is sheathed on the safety protection sleeve and the needle as a whole. The lower portion of the protection sheath is connected to and cooperates with the lower portion of the safety protection sleeve.