Disclosed is a pierceable septum for use in drug reservoirs and infusion sets. The pierceable septum has an elastic core made from a core material and a surround made from a surrounding material. The surrounding material is more rigid than the core material. The elastic core is fully embedded in the surround.

An access port, wherein the access port may include a body having an exterior surface and a chamber defined therein, a bore defined in the body providing fluid communication between the chamber and the exterior surface, a needle in fluid communication with the chamber, a passage defined in the body providing communication between the chamber and the exterior surface, a seal secured within the passage, and an actuator in communication with the needle, configured to move the needle relative to the passage or move the passage relative to the needle.

A septum may include a housing and a hollow body that slides with respect to the housing from a closed position to an open position. The hollow body may include one or more holes. The septum may include a first seal coupled to the distal end and a second seal coupled to the proximal end. In response to the hollow body being in the closed position, the second seal may block a proximal opening of the housing, and the holes may be disposed within the housing. In response to the hollow body sliding from the closed position to the open position, the holes may be disposed distal to the housing, and the second seal may be removed from the proximal opening of the housing such that fluid may flow proximally into the plurality of holes and through the proximal opening of the housing.

Provided herein is a fluid pathway connection assembly, e.g., for connecting a fluid flowpath within a drug delivery device for delivery of a medicament to a target site. The fluid pathway connection assembly comprises a hollow needle piercing member, a sleeve fixedly engaged with the piercing member and a pierceable seal configured to sealingly engage the piercing member or the sleeve. Upon, sealing engagement, the piercing member or the sleeve and the pierceable seal form a volume within which a portion of the piercing member is disposed. The fluid pathway connection assembly is activated by relative movement between the piercing member and the pierceable seal and activation causes the piercing member to pierce the pierceable seal, thereby establishing a fluid flowpath through the pierceable seal. Upon incorporation of the assembly into a sealed fluid flowpath, the volume is isolated from the environment and maintains the sterile condition of the portion of the piercing member disposed therein. Also provided herein are drug delivery pumps and methods of operating and assembling the assemblies and pumps described herein.

An access port for providing subcutaneous access to a patient is disclosed. In one embodiment, the port includes an internal body defining a fluid cavity that is accessible via a septum. A compliant outer cover including silicone is disposed about at least a portion of the body. A flange is included with the port body and is covered by the outer cover. The flange radially extends about a perimeter of the port body proximate the septum so as to impede penetration of a needle substantially into the outer cover in instances where the needle misses the septum. The flange can further include both an anchoring feature for securing the outer cover to the port body and an identification feature observable via x-ray imaging technology for conveying information indicative of at least one attribute of the access port. The outer cover provides a suitable surface for application of an antimicrobial/antithrombotic coating.

A method of preventing blood leakage through a septum of a catheter assembly when a needle is disposed within a slit of the septum may include providing a lubricant within multiple gaps disposed between an outer surface of the needle and the slit. The lubricant may include a viscosity greater than 1,000 centipoise. Providing the lubricant within the multiple gaps may include applying the lubricant to the outer surface of the needle, and inserting the lubricated needle distally through the slit of the septum. Providing the lubricant within the multiple gaps may include applying the lubricant to a tip of a septum actuator of the catheter assembly, and penetrating the septum with the lubricated septum actuator. Providing the lubricant within the plurality of gaps may include dispensing the lubricant within the slit of the septum prior to insertion of the septum into the lumen of the catheter adapter.

A cap assembly includes an access member configured for attachment to a reservoir. The access member includes a first port that enables needleless extraction of contents from the reservoir, and at least one second port that enables needled extraction of the contents from the reservoir. The cap assembly further includes a valve member positioned in or configured to be positioned in the access member to i) enable needleless extraction of the contents of the reservoir through the first port when the first port is attached to a needless extraction device, ii) enable needled extraction of the contents through the at least one second port, and iii) seal the contents of the reservoir at the first port and at the at least one second port prior to and subsequent to the needleless or needled extraction.

An access port for providing subcutaneous access to a patient is disclosed. In one embodiment, the port includes an internal body defining a fluid cavity that is accessible via a septum. A compliant outer cover including silicone is disposed about at least a portion of the body. A flange is included with the port body and is covered by the outer cover. The flange radially extends about a perimeter of the port body proximate the septum so as to impede penetration of a needle substantially into the outer cover in instances where the needle misses the septum. The flange can further include both an anchoring feature for securing the outer cover to the port body and an identification feature observable via x-ray imaging technology for conveying information indicative of at least one attribute of the access port. The outer cover provides a suitable surface for application of an antimicrobial/antithrombotic coating.

A percutaneous access device comprises a frame, a hatch and a hinge that couples the frame to the hatch. The frame has a passageway that extends therethrough. When the percutaneous access device is implanted in a patient, the frame is positioned beneath a layer of skin of the patient against a bodily vessel. Moreover, the hinge biases the hatch closed against the frame in a normally closed position such that liquid flowing through a lumen of the vessel cannot escape through the percutaneous access device. However, the application of force against the hatch from an object (such as a needle) that extends through the passageway causes the hatch to open outwardly from the frame and into the lumen of the vessel. Correspondingly, the hinge biases the hatch back to the normally closed position upon removal of the object.

A catheter system may include a catheter adapter, which may include a distal end, a proximal end, a lumen extending through the distal end and the proximal end, and a side port in fluid communication with the lumen. A catheter may extend distally from the catheter adapter. A septum may be disposed within the lumen. The septum may include a first slit generally aligned with a longitudinal axis of the catheter and a second slit offset from the longitudinal axis of the catheter. An introducer needle may be secured within a needle hub and may extend through the catheter and the first slit of the septum. A winged needle set may include: a body; a needle extending distally from the body and through the second slit of the septum; an extension tube extending from the body; and a blood collection device coupled to the extension tube.