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.

A connector hub for a needle assembly, the connector hub comprising a first portion located at a first end section of the connector hub, the first portion comprising a first longitudinal axis, a second portion located at a second end section of the connector hub opposite the first end, the second portion comprising a second longitudinal axis, a medial portion located at a middle section of the connector hub between the first and second end sections, the medial portion comprising a medial longitudinal axis arranged at an angle relative to the first longitudinal axis, and arranged at an angle relative to the second longitudinal axis, and at least one insertion port located on the medial portion, wherein the insertion port comprises an insertion port longitudinal axis, wherein the insertion port longitudinal axis is arranged at an angle relative to the medial longitudinal axis.

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.

A method for controlling intraocular pressure in a patient’s eye is provided. The method includes creating an intraocular entry into the eye, selecting a location along an optical disc of the eye, creating a conduit connecting at least a portion of an intravitreal cavity with at least a portion of a subarachnoid space in the eye at the selected location, deploying at least one stent communicating between the intravitreal cavity and the subarachnoid space via the conduit, and equilibrating the intraocular pressure in the eye by allowing the stent to communicate fluid flow between the intraocular compartment and the subarachnoid space.

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 stabilizing connector includes a connector portion and a stabilization portion. The connector portion is configured to couple to an access device. The connector portion defines at least one lumen that is configured to be placed in fluid communication with a lumen of the access device. The stabilization portion is coupled to the connector portion. The stabilization portion is configured to be placed in contact with a surface of a patient's skin to stabilize at least one of the stabilizing connector or the access device.

Valve devices are provided for draining fluids from and/or infusing fluids into a patient's body that include a housing including first, second, and third connectors, a primary fluid path communicating between the first and second connectors, and a secondary fluid path communicating from the primary fluid path to the third connector. First and second valve members are movable within the housing between first positions wherein the valve members do not obstruct the primary fluid path and second positions wherein the primary fluid path is at least partially closed. The third connector may be configured to prevent fluid flow therethrough unless a mating connector is fully coupled thereto. The valve members may be selectively closed to isolate portions of the flow path to allow a source of vacuum or fluid coupled to the third connector to aspirate or infuse fluid along portions of the primary fluid path.

An apparatus includes an introducer defining a lumen and a catheter movably disposed in the lumen. The introducer has a distal end portion configured to operably couple to an indwelling peripheral intravenous line at least partially disposed in a vein. The catheter is configured to be moved between a first position, in which the catheter is proximal to the peripheral intravenous line when the introducer is operably coupled thereto, and a second position, in which a distal surface of the catheter is distal to the introducer and disposed at a predetermined distance from a distal tip of the peripheral intravenous line. The predetermined distance defined between the distal surface of the catheter and the distal tip of the peripheral intravenous line is based at least in part on a venous anatomy associated with the vein.