A tamper resistant catheter device preventing unauthorized access, while permitting authorized intravenous medications through an inlet port. The device comprises a catheter line retainer having a base supporting the catheter line, a lumen adaptor engaged with the catheter line, and a locking clamp for clamping the catheter line within the catheter line retainer. An installation tool is provided having a breakaway handle and a locking cap for covering the lumen adaptor. Finally, a slotted retaining sleeve is installed using the breakaway handle of the installation tool for engagement with the locking cap and around the lumen adaptor. The slotted retaining sleeve engages the locking clamp to block removal of the locking clamp from the line retainer. Once the slotted retaining sleeve and locking cap are installed, the breakaway handle is removed. A removal tool disengages the locking cap from the slotted retaining sleeve for authorized access.

A seal for a hemostasis valve is provided as well as a novel seal stack for use in hemostasis valves. The seal stack includes a plurality of conical or frustoconical members including an anti-prolapse member, and a sealing member. The seal stack may optionally include a diaphragm and/or a second sealing member. The valve body may include a pressure sensing member which may be located in a sidearm.

A hemostasis valve hub for use with an introducer sheath includes a base having a securing mechanism for securing the hemostasis valve hub to the introducer sheath, an outer shell securable to the base and defining an interior volume, a shutter helix section disposed within the interior volume and including a plurality of fins arranged in a helical fashion, a brush section disposed within the interior volume adjacent the disk shutter section, the brush section including a plurality of brushes arranged in a helical fashion, and a seal positioned within the base and adjacent the brush section, the seal having a partial cross slit arrangement.

This patent document discloses devices and associated methods for catheter and guidewire management in a surgical setting. Implementations can include a hemostasis valve configured to prevent the backflow of blood during a medical procedure. The hemostasis valve can have a valve body defining an inner lumen extending from a proximal end of the body to a distal end of the body. The inner lumen can be configured to accommodate passage of one or more elongate interventional devices therethrough. An interventional device management component can be positioned at the proximal end of the valve body. The interventional device management component can comprise a body defining a first seal member lumen configured to receive a first elongate interventional device and a second seal member lumen configured to receive a second elongate interventional device. A narrow slit configured to receive a guidewire can connect the seal member lumens.

An introducer for insertion of a medical device into a patient's vasculature includes an elongate introducer body, a hub, and a hemostatic valve. The elongate introducer body includes a longitudinal axis, a proximal region, a distal region, and an inner lumen. The hub is coupled to the proximal region of the introducer body. The hemostatic valve is disposed within the hub and forms a liquid-tight seal across the inner lumen. The introducer includes a guide configured to guide an object towards the center of the valve during insertion of the object.

Aspects herein relate to a low-friction septum for providing a leak-resistant seal for use in a vascular access device. In an embodiment, a device for vascular access hemostasis is included having an enclosure defining a cavity and configured to at least partially receive a medical device. The device can include a first seal portion and a second seal portion, the cavity disposed between the first seal portion and the second seal portion. The device can include a barrel in structural communication with the second seal portion, the second seal portion including a septum seal. The second seal portion can define two or more discrete portions, each separated by one or more split lines. The discrete portions can include a mating surface to interface with mating surfaces of other discrete portions. The mating surface can include a surface topology including raised portions and depressions. Other embodiments are also included herein.

A catheter assembly is disclosed that includes a catheter adapter having a port disposed on its sidewall. A valve is coupled to the port to seal the opening in the port.

A vascular access system which may be configured for blood draw may include a housing, which may include a distal end, a proximal end, and a slot disposed between the distal end and the proximal end. The slot may include a notch. The vascular access system may include a cannula hub, which may be disposed within the housing and movable with respect to the slot. The cannula hub may include a tab extending through the slot. The vascular access system may include a cannula extending distally from the cannula hub. In response to the tab being disposed within the notch, a distal tip of the cannula may be disposed within the housing. In response to advancing the tab along the slot to a distal end of the slot, the distal tip of the cannula is disposed distal to the distal end of the housing.

A hemostasis valve for use with catheters in intravascular procedures. The hemostasis valve comprising a sealable fluid channel that bifurcates from a single distal lumen to two proximal lumens. An upper proximal lumen may include a funnel shaped opening to improve aspiration potential. Rotating locking mechanisms are attachable at the ends of the hemostasis valve to interlock coaxial devices or to form seals around coaxial devices. Injection molding may be used to manufacture a hemostasis valve and its components. A mold and core pins may impart external and internal shapes to a molten polymer. Once the polymer has cooled, the molded component is separated from any pins or molds and attached to other molded components to form an assembled hemostasis valve.

A catheter priming apparatus may include a barrier forming a reservoir. Fluid may be disposed within the reservoir. A support structure may be disposed within the barrier. The support structure may include an opening extending through the support structure and a connector configured to couple the catheter priming apparatus to a catheter system. A one-way valve may be coupled to the support structure and configured to allow the fluid to flow out of the reservoir through the connector in response to compression of a portion of the barrier aligned with the opening.