Vascular access catheter comprising elongated tubular catheter body enclosing a lumen. Catheter body includes catheter tip ending with a catheter distal end and comprising a distal edge at the catheter distal end surrounding an opening opened to the lumen. he distal edge includes a front edge portion spanning a top portion of the opening and an inclined edge portion spanning a bottom portion of the opening and inclining proximally away from the front edge portion, relative to a longitudinal axis of the catheter body. The vascular access catheter can be provided in a vascular access kit further comprising access needle with hollow needle body and beveled tip ending with sharp needle edge.

A port is adapted to be implanted to a body with its top exposed to the environment. The port has a housing defining a chamber that has an opening at the top of the housing. An aperture having a lumen attached thereto is formed at the lower portion of the chamber. For infusion, an insert that has an internal passageway that connects a fluid inlet at its top surface and a bore at its sidewall is sealingly mated to the chamber. The bore sealingly aligns with the aperture. After infusion, the insert is removed, and a blank insert is fitted to the chamber. A band of tissue ingrowth media encircles the housing to form an aseptic barrier where the outer wall of the housing and the tissue of the body encircling the housing meet.

A therapeutic delivery device that provides a controlled release of high doses of a therapeutic agent in a local area, sustains the high dose controlled release with a percutaneous port for refilling the device, and is versatile for use with multiple types of therapeutic agents and/or implant systems. A rate determining/controlled release membrane is used to decrease the molecular mobility of the therapeutic compounds thereby controlling the therapeutic release profile. The therapeutic delivery device includes a body defining an internal reservoir for receiving a therapeutic agent and including a first membrane for providing a controlled release of the therapeutic agent to the surgical site, a port in fluid communication with the reservoir, a sleeve configured to encapsulate the body, and a rigid housing configured to support the body and a portion of the sleeve, the rigid housing configured to release the body and the sleeve after the body and the sleeve are anchored position relative to the surgical site.

Catheters, vascular access devices using such catheters, methods of using such catheters and uses of such catheters are disclosed. The catheter comprises polymeric tubing including a composition that can be magnetized by application of an externally applied magnetic field, thereby magnetizing the tubing. Detection of the magnetic field provides location information for the catheter in the vasculature.

Systems, methods and devices are described including a catheter adapter subassembly including a magnetic feature. Systems include such a catheter adapter subassembly and a needle subassembly including a magnetic feature, and relative movement of the catheter adapter subassembly and the needle subassembly can be determined using a magnetometer.

An improved method and device are provided for forming and/or maintaining a percutaneous access pathway. The device generally comprises an access pathway and attachment device. The provided assembly substantially reduces the possibility of iatrogenic infection while accessing and/or re-accessing a body space.

A septum for a port is provided, the septum having a top wall and a side wall. The side wall can include a pressure-activated valve element for regulating the flow of fluid across the valve. The curvature of the side wall and the geometry of the sidewall and the housing can be tailored to bias the valve element to open at different pressures during infusion and aspiration. The side wall can also include an extended portion that can function as a suture wing for securing the port within a port pocket.

Dural repair devices that are configured to effectively and reliably repair the damage of a dural tear due to incidental durotomies are provided, along with methods of use. The devices and methods enhance the ability of a surgeon to repair a patients dura mater, or dura, during surgery of the central nervous system. The dural repair device has a multi-layer structure configured to exert a pressure or tamponade effect to compress a patient's dura to its state prior to the spinal surgery. Thus, the dural repair devices and methods of use may reduce the patients risk morbidity, further surgery, spinal headaches, or other injuries and discomforts.

A delivery adapter which may be used as an interface between a syringe and a catheter hub is described.

A device for positioning a subcutaneous port during an access procedure, said device comprising a dome (1) of plastic material, said dome being shaped to fit directly over the subcutaneous port, and a flange (3) extending laterally from the dome which is able to contact a surrounding skin area, wherein the device is a unitary device which is configured to be deformable or fracturable so as to facilitate removal of the device from the surrounding skin area.