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.

A bleed-back control valve is provided having a sidearm and an integrated three-way stopcock switching between two alternative fluid paths. One of the alternative fluid paths communicates with an inline pressure transducer embedded in the wall of the sidearm. The bleed-back control valve also includes a purge valve located near the blunted apex of a conical seal located in the main valve body. The purge may be opened to expel air from the space around the blunted apex.

A system for providing vascular access in a patient's body may comprise at least one hemostatic valve and at least one clamp to be used with a vascular graft. The vascular graft comprises a tubular body having a proximal end and a distal end, the proximal end being configured to be attached to a vessel in a patient's body. The at least one valve is configured to be attached to the distal end of the graft's tubular body and comprises a housing including a flexible membrane that allows a medical device to be inserted through the membrane into said vascular graft. The valve further comprises an introducer sheath configured to be inserted into the distal end of the graft's tubular body. The at least one clamp is configured to be disposed around the graft's tubular body and has a first configuration that allows insertion of the valve's introducer sheath into the distal end of the graft's tubular body and a second configuration that allows clamping of the graft against the valve's introducer sheath, when inserted in the graft's tubular body.

A cannula for use in an access assembly includes an instrument valve housing including first and second housing sections and defining a cavity and a valve assembly disposed within the cavity of the instrument valve housing. The valve assembly includes a seal assembly including an outer flange and a septum seal extending across the outer flange, a guard assembly disposed within the outer flange of the seal assembly, and a centering mechanism. The guard assembly includes a plurality of guard members. Each guard member of the plurality of guard members includes a ring portion and a flap portion. The flap portions of the guard members of the guard assembly are configured to engage and stretch the septum seal during reception of a surgical instrument through the valve assembly.

A system for providing vascular access in a patient's body may comprise at least one hemostatic valve (610) and at least one clamp (210) to be used with a vascular graft (110). The vascular graft (110) comprises a tubular body having a proximal end (110A) and a distal end (110B), the proximal end (110A) being configured to be attached to a vessel in a patient's body. The at least one valve (610) is configured to be attached to the distal end (110B) of the graft's tubular body and comprises a housing (616) including a flexible membrane (611) that allows a medical device (810) to be inserted through the membrane (611) into said vascular graft (110). The valve (610) further comprises an introducer sheath (615) configured to be inserted into the distal end (110B) of the graft's tubular body. The at least one clamp (210) is configured to be disposed around the graft's tubular body and has a first configuration that allows insertion of the valve's introducer sheath (615) into the distal end (110B) of the graft's tubular body and a second configuration that allows clamping of the graft (110) against the valve's introducer sheath (615), when inserted in the graft's tubular body.

Collapsible tube embodiments may be used to promote hemostasis at surgical sites or any other suitable location. In some cases, vascular closure device embodiments may include collapsible tube embodiments in order to promote hemostasis at a surgical site during a vascular closure procedure.

A hemostasis valve device includes a valve body having an open first end and an open second end with a main lumen extending from the open first end to the open second end. The valve includes a valve member disposed within the main lumen of the valve body at or proximate to the open first end, the valve member having an open position and a closed position. An actuator is disposed between the valve member and the open second end. The actuator is configured to move the valve member between the open position and the closed position.

A tightening port for use with a hub of an introducer sheath includes a cartridge for reversible engagement with a proximal end of the hub, the cartridge having a proximal end and a distal end and a lumen extending therebetween, a seal positioned within the lumen of the cartridge, a lock nut having an inner portion positioned within the lumen of the cartridge and an outer portion configured for engagement with the proximal end of the cartridge, such that the inner portion of the lock nut is configured to push the seal to reduce a size of an opening of the seal.

Disclosed herein is a system for treatment including a compound valve system that can be integral to, or attached to a sheath introducer. The compound valve system includes a secondary valve that can be positioned in a proximal direction from a primary valve of the sheath introducer. The secondary valve can move longitudinally in response to a pressure differential. The compound valve system can include an aspiration port between the primary valve and secondary valve. The secondary valve can be integral to a secondary valve accessory device that can be assembled onto a catheter shaft of an intralumenal treatment device, and the secondary valve accessory device can further function as an introducer tool for the intralumenal treatment device.

A catheter assembly comprises a catheter (18), a needle (12) having a sharp distal tip disposed within the catheter (18), a catheter hub (14) connected to the catheter (18) having the needle (12) passing therethrough, the catheter hub (14) including a valve (38) that selectively permits or blocks a flow of fluid through the catheter (18), a valve actuator (54) that moves between a first position and a second position, and a return member (56) that returns the valve actuator (54) from the second position to the first position, and a needle protection member (176) that encloses the sharp distal tip of the needle (12).