Systems and connectors for hemostasis valves and associated methods are disclosed herein. According to an aspect, a connector for a medical device includes a body defining a first opening, a second opening, and a channel. The channel provides passage between the first opening and the second opening. The body is configured to engage an inlet port of a hemostasis valve at the first opening when the body and the hemostasis valve are arranged in one or more positions with respect to each other. The connector also includes a clip attached to the body and configured to fasten the body to the hemostasis valve when the body and the hemostasis valve are arranged in one of the positions.

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.

Hemostasis valve devices and methods of use are disclosed. The hemostasis valve devices include a body member, a slide member, an introducer member, a valve cap, and a valve member. The body member and slide member can be gripped by a user's finger and thumb, respectively. The slide member can be distally displaced by the user's thumb to distally displace the introducer member through the valve member to open the valve member to allow passage of a medical appliance through the valve member. The introducer member can be selectively locked in a distal position to keep the valve open.

Vascular filters and deflectors and methods for filtering bodily fluids. A blood filtering assembly can capture embolic material dislodged or generated during an endovascular procedure to inhibit or prevent the material from entering the cerebral vasculature. A blood deflecting assembly can deflect embolic material dislodged or generated during an endovascular procedure to inhibit or prevent the material from entering the cerebral vasculature.

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 vasculature navigation system may include a dilator having a proximal end and a distal end located opposite the proximal end, the dilator comprising a guidewire lumen extending between the proximal end and the distal end, the dilator defining a proximal portion and a distal portion located opposite the proximal portion. In some embodiments, the vasculature navigation system also includes an access port located at the proximal end of the dilator, a distal port located at the distal end of the dilator, and a hemostasis valve coupled to the proximal portion of the dilator. The hemostasis valve may be configured to control fluid flow between the proximal portion and the distal portion. In some embodiments, a flush port is coupled to the proximal portion of the dilator and located distal to the hemostasis valve, and the flush port is coupled to a fluid supply source.

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.

Devices, systems, and methods for sealing medical devices, particularly during intravascular access, are disclosed herein. Some aspects relate to a hemostatic valve for sealing a wide range of medical devices, such as catheters, wires, embolectomy systems. The valve can include an elongate member having a first end, a second end, and a central lumen extending therebetween. A reinforcement structure extends along at least a portion of the elongate member and is coupled to the elongate member. A shell defining a first aperture and a second aperture may be included, which first and second apertures can be fluidly coupled by the elongate member. A tensioning mechanism is coupled to the shell and to the elongate member, the tensioning mechanism can be moveable between a first configuration wherein the tensioning mechanism is collapsed and the central lumen is sealed and a second configuration wherein the central lumen is open.

A clamping device for a shaft of a catheter can include a first member rotatably coupled to a second member. The first member can have an annular element defining a central lumen, the outer surface of the annular element having a non-circular cross-sectional profile, and the second member can define a bore into which the annular element extends, the bore having a non-circular cross-sectional profile. The device can move between a release state wherein the central lumen has a first diameter, and a clamped state wherein the central lumen has a second diameter less than the first diameter. When the clamping device is in the clamped state, the clamping device can engage an outer surface of a catheter shaft and when the clamping device is in the release state, the clamping device can be moved along a length of the catheter shaft.

According to one aspect of the disclosure, a delivery device may include a handle, a catheter sheath extending distally from the handle, and a hemostasis valve positioned within the handle. The hemostasis valve may be located proximal to the catheter sheath and distal to a proximal end of the handle. The delivery device may also include a hemostasis bypass assembly coupled to the handle. The hemostasis bypass assembly may include a bypass tube coupled to an actuator. The actuator may be configured to be transitioned between a first condition in which a distal end of the bypass tube is positioned proximal to the hemostasis valve and the hemostasis valve is closed, and a second condition in which the distal end of the bypass tube traverses the hemostasis valve and the hemostasis valve is opened.