A61M39/0613

HEMOSTASIS VALVES AND METHODS OF USE
20220347455 · 2022-11-03 ·

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.

Aspiration system with accelerated response
11259821 · 2022-03-01 · ·

An aspiration system exhibits an accelerated drop in negative pressure at the distal end of an aspiration catheter from the time of opening a valve. The system includes an aspiration pump in communication with a first chamber, and an aspiration catheter configured for placement into fluid communication with the first chamber by way of an elongate aspiration tube. A second chamber is provided between the aspiration tube and the catheter, and a valve is provided between the second chamber and the aspiration catheter. Upon opening of the valve with negative pressure at equilibrium in the first and second chambers, resistance to fluid flow between the second chamber and the distal end of the catheter is less than the resistance to fluid flow between the second chamber and the first chamber, causing a rapid aspiration into the second chamber.

VASCULAR ACCESS
20170312492 · 2017-11-02 ·

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.

Trocar assembly

A surgical system comprising a cannula assembly and an obturator assembly for penetrating tissue is disclosed. A cover of the cannula assembly is mounted to a cannula housing and has a cover aperture therethrough. The cover has a trailing end face defining a predetermined geometrical configuration, at least a portion of the trailing end face is obliquely arranged relative to a longitudinal axis and terminates in, and leads toward the cover aperture to facilitate guiding of the surgical object through the cover aperture. The obturator assembly includes an obturator housing and an obturator member. The obturator housing has a housing base defining a leading end face, which defines a predetermined geometrical configuration corresponding to the predetermined geometrical configuration of the trailing end face of the cover to mate therewith upon assembly of the obturator assembly with the cannula assembly.

DELIVERY SYSTEMS WITH INTRODUCER AND DISTAL SHEATHS AND METHODS OF USE
20170281382 · 2017-10-05 ·

A delivery system and method of its use delivers a stent graft prosthesis to a surgical site, such as an abdominal, thoracic or thoraco-abdominal aortic aneurysm. The delivery system includes a handle defining a conduit, an introducer sheath extending distally through the handle, a substantially straight inner control tube extending through the conduit of the handle and from the distal end of the introducer sheath, and a distal sheath that extends through and beyond a distal end of the introducer sheath. The distal sheath can have, in one embodiment, a diameter equal to or less than that of the introducer sheath. Retraction of the distal sheath through the introducer sheath and the handle exposes a stent graft prosthesis extending about the inner control tube. Removal of the inner control tube from the introducer sheath allows for implantation of additional components through the introducer sheath.

MEDICAL VALVE WITH A VARIABLE DIAMETER SEAL
20170281920 · 2017-10-05 ·

A medical valve assembly includes a tube extending between a first tube end and a second tube end to define a passageway extending along a longitudinal axis between the ends. A plunger plate extends radially from the second tube end of the tube, and a valve housing surrounds the tube about the second tube end and extends from a first valve housing end to a second valve housing end. The valve housing includes a housing flange extending radially inwardly from the second valve housing end and disposed in spaced relationship with the plunger plate to define a distance dimension D extending therebetween. An elastomeric seal is compressed between the plunger plate and the housing flange, and one of the valve housing and the tube is axially movable relative to the other to vary the distance between said plunger plate and said housing flange and adjust an inner diameter of the elastomeric seal.

SECUREMENT DEVICES FOR INTRACARDIAC BLOOD PUMP SYSTEMS

Improved securement devices for use with intracardiac blood pump assemblies are provided. The present technology provides securement devices that may be used with a sheath assembly (e.g., an introducer sheath assembly, repositioning sheath assembly), and which are configured to restrict movement of an object (e.g., the catheter of the pump assembly) within the sheath assembly except when a mechanism (e.g., button) of the securement device is actively being actuated (e.g., pressed, held, etc.).

Catheter assemblies with valves and related methods
09764085 · 2017-09-19 · ·

Needle assemblies with valves and related methods are disclosed. An exemplary needle assembly includes a needle hub with a needle attached to a distal end of the needle hub and a catheter hub having a wall structure defining an interior cavity and a catheter tube extending distally therefrom having the needle projecting through the catheter tube. A valve with a cylindrical walled structure and a disc with a plurality of slits and flaps are located in the interior cavity of the catheter hub in which the cylindrical walled structure defines an open proximal end. A plurality of flexible ribs can be included and connect to an interior wall surface of the cylindrical walled structure and the disc with an actuator disposed inside the interior cavity of the catheter hub and having a distal end sized and shaped to project into the open proximal end of the valve.

COLLAPSIBLE TUBE FOR HEMOSTASIS
20220039781 · 2022-02-10 ·

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.

INSERTING MEMBER FIXING DEVICE
20210402150 · 2021-12-30 ·

This device is an inserting member fixing device to fix a linear inserting member to an insertion target, the inserting member fixing device comprising: a main body; a chuck portion; an inner sealing portion to be brought into close contact with an outer periphery of the inserting member; an inserting member supporting portion to support the inserting member; and a movement restricting portion to restrict movement of the inner sealing portion and the inserting member supporting portion. The inserting member supporting portion and the inner sealing portion are provided adjacent to each other in an axial direction of the inserting member, and a space is provided between the inserting member supporting portion and the inner sealing portion so that a main body-side end portion of the inserting member supporting portion is displaceable when the inserting member swings.