A cannula hub includes a shaft mount segment and a cannula coupling segment. A set of coupling nubbins radially extend from the outer surface of the cannula coupling segment. The coupling nubbins are aligned with one another along a helical cannula coupling pathway on the outer surface and are adapted to be received within a cooperative helical groove on a transfer vessel. The coupling nubbins have a protrusion projection distance that is greater than the depth of the groove. When a sufficient rotational force is applied to the cannula hub, the coupling nubbins score the inside face of the groove which increases the groove depth and enables the coupling nubbins to advance along the groove while forming a tight compression fit of the coupling nubbins within the groove.

A cleaning device is configured access and remove fluid from and dry a moat region defined by a hub of a medical connector, thereby minimizing the potential for bacterial growth in the hub. The cleaning device takes the form of an absorbent block which can be inserted into the moat by extending about a central male fitting and into a gap between the male fitting and the inner wall of a female hub of the medical connector. In a preferred embodiment of the invention, the block takes the form of a tubular cylinder particularly configured for use on ENFit medical connectors wherein the absorptive feature of the cleaning device can be employed alone or in combination with another cleaning tool used to first remove any existing dried and caked solution in the hub before removing residual cleaning fluid from the moat.

Cap and cleaning devices antiseptically maintain patient fluid line access valves to minimize the risk of infection via catheters. The devices have a cap that may contain a dry pad impregnated with an antimicrobial agent. The cap covers the access portion of the access valve when not in use. The devices have a hood that contains a wet pad impregnated with a cleaning solution and, optionally, an antimicrobial agent. The wet pad cleans the access portion of the access valve prior to and optionally, after the access valve is utilized to access the patient fluid line.

An antiseptic medical cap that may include a base, a sidewall, and a chamber configured to receive a proximal end of a medical fluid port having an opening. The antiseptic medical cap, in some instances, may include an insert having a gas-releasing anti-microbial compound and/or include a nitric oxide-releasing system that is configured to be positioned at least partially through the opening of the medical fluid port when the antiseptic medical cap receives the proximal end of the medical fluid port into the chamber.

A housing includes a cavity portion and a cover portion configured for rotary motion. The cover portion can include a receiver port configured to engage with a fitting configured for coupling to an end of a first tube. At a first alignment position of the cavity portion relative to tire cover portion, the receiver port is aligned with a first retention cleat. At a second alignment position of the cavity portion relative to the cover portion, the receiver port is aligned with a fluid coupler. At a third alignment position of the cavity portion relative to the cover portion, the fitting is aligned with a second cap.

A syringe assembly including: (1) a syringe barrel defining a chamber; (2) a plunger mounted in the chamber and moveable with respect to the barrel; and (3) a cap holder assembly containing a cap and an absorbent material removably attached to the syringe.

There is provided an IV flow regulator including a first part integrated with a flow control slit, the flow control slit being along a fluid path; a second part integrated with a central stem, the central stem including a spiral surface configured to contact the flow control slit, an area of contact defined by the spiral surface and the flow control slit being shaped substantially like an orifice to enable flow along the fluid path; and a dead space chamfer included in the second part at a portion of the fluid path subsequent to the area of contact.

The medical liquid collection tip (1) includes a male member (11) that is to be inserted into a tube end (154) of an injector (150) at one end, and includes a liquid collection needle (20) at the other end. A flow path (8) penetrates through the tip (1) in a lengthwise direction thereof and causes the male member (11) and the liquid collection needle (20) to be in communication. The outer circumferential surface (12) of the male member (11) is a male tapered surface with an outer diameter that becomes smaller as the leading end is approached, and is configured to be fluid-tightly connected to the female tapered surface of the tube end (154).

A set connector assembly for a fluid infusion device is provided. The set connector assembly includes a connector having a body. The body defines a graspable portion and a coupling portion, and the coupling portion is to be received within a portion of the fluid infusion device. The graspable portion has at least one locking tab to lock the connector to the fluid infusion device, and the graspable portion is movable relative to the body to move the connector between a first, locked position and a second, unlocked position relative to the fluid infusion device.

A fluid infusion device is provided. The fluid infusion device includes a housing that includes a lock and a set connector assembly removably coupled to the housing to define a fluid flow path from the fluid infusion device. The set connector assembly includes a connector having a body that defines a graspable portion and a coupling portion. The coupling portion is receivable within the housing, and the graspable portion has at least one wing that defines a locking tab for engaging the lock. The at least one wing is movable relative to the body to disengage the locking tab with the lock.