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.

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.

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.).

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 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.

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.

A medical valve assembly includes a tube extending between proximal and distal tube ends. A plunger plate extends radially from the distal tube end, and a valve housing surrounds the tube and extends between proximal and distal valve housing ends. The valve housing includes a flange extending radially inwardly from the distal 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 flange to establish a closed condition of the medical valve assembly. The elastomeric seal axially moves one of the valve housing and the tube relative to the other when a medical device is inserted into the medical valve assembly to automatically increase the distance dimension and establish an open and sealed condition of the medical valve assembly with the inserted medical 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.

A bubble for use with various medical equipment or other sites on the body such as IV ports, feeding tube locations, PODs, CGMs (Continuous Glucose Monitors) or other equipment connected to the body, whereby the bubble assists in protecting the site, and hopefully prevents medical equipment from being dislodged, if installed, to provide for strenuous activity or even application of water, such as bathing, showering, etc.

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.