A catheter assembly may include a catheter adapter, a septum housing, and a septum. The catheter adapter may include a distal end, a proximal end, an inner wall extending between the distal end and the proximal end, and a lumen formed by the inner wall. The septum housing may include one or more protrusions and may be secured to the inner wall by one or more of the following: an interference fit between the one or more protrusions and the inner wall, a snap fit between the one or more protrusions and the inner wall, and bonding between the one or more protrusions and the inner wall. The septum may be at least partially disposed within the septum housing and configured to at least substantially seal the lumen.

The fluid delivery devices, systems and methods described herein include a subcutaneous port, a catheter, and a connection assembly configured to fluidly couple the port and catheter.

A dual reservoir access port includes a base having proximal and distal fluid reservoirs. The fluid reservoirs each comprise a bottom and a side wall. A dual prong outlet stem projects from a distal end of the base and comprises a first prong and a second prong. A first fluid channel extends through the first prong to the distal reservoir, and a second fluid channel extends through the second prong to the proximal fluid reservoir. A puncture shield is disposed between at least a portion of the second fluid channel and the bottom of the distal fluid reservoir. A needle-penetrable septum is disposed atop of each of the fluid reservoirs. A cap is placed over and around the port base compressing and sealing the septa against the base. A locking collar may be placed over a dual lumen catheter to lock the catheter to the dual prong outlet stem.

The invention relates to a coupling component for a fluid coupling (1) for releasably connecting fluid-conveying components, in particular fluid-conveying components in medical equipment, wherein the coupling component comprises a coupling housing (14) through which a fluid channel (17) passes in regions and which is provided with a coupling recess (7) that is sunken into a surface (15) of the coupling housing (14), wherein a channel opening (18) of the fluid channel (17) ends at an end face (19) of the coupling recess (7). According to the invention, it is provided that the channel opening (18) is covered by a membrane seal (4) which is made of a resilient material and through which a fluid gap passes (8) that is designed such that the membrane seal (4), when in a resting position, seals the channel opening (18) and, when in an operative position, opens the channel opening (18), wherein at least one yielding depression (29) is formed in the coupling recess (7) adjacently to the channel opening (18), which depression is designed for an yielding movement of a region (36, 37) of the membrane seal (4) when the membrane seal (4) transitions from the resting position into the operative position.

Hemostasis valves and hemostasis valve assemblies can be coupled to a proximal end of an introducer sheath to prevent blood loss through the proximal end of the introducer sheath. Some hemostasis valve assemblies may include an elastomeric member with a variable-width channel that is designed to form a liquid-tight seal over elongate members of different diameter or a single elongate member of variable diameter.

A piston for a needleless valve system comprising a head portion configured to be disposed in the needleless valve system and controlling fluid flow through the needleless valve system. The head portion comprising a continuous top surface, and an opening disposed proximate the continuous top surface, wherein the continuous top surface is non-planar when the opening is in an open position.

A device for the thorough delivery of liquid medicine in an intravenous (IV) delivery system. The device consists of a negative pressure chamber filled with saline solution that is used to flush all of the residual liquid medicine from a secondary liquid medicine delivery tube. The negative pressure chamber sits below the drip chamber attached to the secondary medicine bag and is attached to the secondary medicine delivery tube in such a way that when the liquid medicine from the delivery tube has flowed below the negative pressure chamber, the negative pressure chamber releases the stored saline to flush the liquid medicine from the secondary liquid medicine delivery tube.

An access port includes an access port body and a needle-penetrable septum. The access port body can be of integral single-piece construction, and can define a reservoir aligned with an access opening. The access port body can further define an annular groove between the reservoir and the opening. The annular groove can have a diameter greater than a diameter of the access opening and a diameter of the reservoir. The needle-penetrable septum can include an upper portion disposed in the access opening and an annular flange disposed in the annular groove. The annular flange can extend radially outward from a lower portion of the septum, and can have a diameter greater than a diameter of the upper portion of the septum. The needle-penetrable septum can further include an annular reinforcement structure disposed within the annular flange.

Aspects herein relate to a medical device for providing a leak-resistant seal for use in a vascular access device. In various embodiments, a device for vascular access hemostasis is included. The device can include an enclosure configured to at least partially receive a medical device, the enclosure defining a cavity. The enclosure can have a first seal portion and a second seal portion, the cavity disposed between the first seal portion and the second seal portion. The enclosure can include the second seal portion comprising a split, septum seal. The enclosure can include a barrel in structural communication with the second seal portion. The device can include a constriction ring disposed around the barrel, the constriction ring interfacing with the second seal portion to limit movement of the split, septum seal.

Embodiments of the present invention provide a vent arrangement integrated with a refill port disposed on the outer shell of an implantable drug-delivery device. The vent arrangement may utilize a tiered structure with two septums in a space-efficient configuration that facilitates both venting of pressure and refill of the drug reservoir.