A method for producing a guidewire, the method includes producing a position sensor by providing a shaft-section having a solid profile, which is sized and shaped to move in an anatomical material transportation system. A wire is wound around an axis of the shaft-section and first and second ends of the wire are coupled to respective first and second locations on an outer surface of the shaft-section. A guidewire-shaft is provided, and the position sensor is coupled to a distal end of the guidewire-shaft.

In some examples of a method of forming a catheter, a structural support member is positioned over an inner liner. Prior to being positioned over the inner liner, the structural support member tapers in diameter along at least a portion of a length of the structural support member.

The present invention relates to a perfusion balloon catheter that has an expandable (enlargeable) inner lumen with a novel design feature that allows a continuous flow through this enlarged lumen sufficient perfusion to the distal lumen of the blood vessel or air passage concurrent to and independently of balloon inflation or deflation resulting in the prolonged dilatation and avoiding the high risks of blood or air flow stricture during balloon inflation.

Devices and methods for establishing trans-radial access for medical intervention are described. In particular, some embodiments are optimized for consistently safely achieving complete cerebral angiography via a single trans-radial access site. A system may include a catheter with at least two active steering sites. Some embodiments may include at least one balloon. The methods include using said steering mechanisms to help guide and support said catheter. In some embodiments, additional use is made of at least one vascular arch to provide further support and prevent kickback and prolapse of said catheter and any additional devices passed therethrough.

A steerable catheter suitable for left-hand operation includes a tube, a handle assembly, and a Luer connector. The handle assembly comprises a holding handle, a slide mechanism, and a slide control mechanism; a proximal end of the tube passes through a cavity of the holding handle to be connected with the Luer connector; the slide mechanism comprises a slide base body, and a slide member axially sliding along the holding handle and fitted on the slide base body; the slide member is fixedly connected to a pull wire; the slide control mechanism comprises a connecting member connected with the slide member, and a drive adjustment member connected with the connecting member and adjusting the position of the slide member; the drive adjustment member is provided at the proximal end of the holding handle for convenient left hand operation.

The present invention relates to a fluid vessel insertion device comprising a) a puncture member arranged for location within a cannulation sheet and comprising an interior lumen; b) a retractor arranged to actuate the puncture member relative to the cannulation sheet in use between i) a first situation in which a distal end of the puncture member protrudes beyond an end of the cannulation sheet, and ii) a second situation in which the distal end of the puncture member is within the cannulation sheet; c) a chamber in fluid communication with an exterior of the device only via the lumen and distal end of the puncture member; and d) a sheet of material located in the chamber to prevent the proximal end of the puncture member from moving; wherein the distal end of the puncture member is configured as a puncturing end having a distal n end opening for insertion into a fluid vessel when in use, and wherein the retractor triggers retraction of the puncture member between the first and the second situation automatically in response to wetting of the sheet of material by a fluid entering the puncture member lumen, whereby the sheet of material is comprising a material whose tensile strength is reduced upon contact with the fluid, and breaks under the pressure of the retractor.

Systems and methods for the intravascular treatment of clot material within a blood vessel of a human patient are disclosed herein. A method in accordance with embodiments of the present technology can include, for example, positioning a distal portion of a catheter proximate to the clot material within the blood vessel. The method can further include coupling a pressure source to the catheter via a tubing subsystem including a valve or other fluid control device and, while the valve is closed, activating the pressure source to charge a vacuum. The valve can then be opened to apply the vacuum to the catheter to thereby aspirate at least a portion of the clot material from the blood vessel and into the catheter.

A medical device that delivers therapeutic agent to the tissue within the bodily passageway while simultaneously permitting flow of bodily fluids past the location of treatment. The medical device includes an inflatable balloon and optionally one or more balloon wall openings that are configured to allow fluid in the interior of the inflatable balloon to flow through the inflatable balloon when the inflatable balloon is pressurized by the fluid in the interior of the inflatable balloon. During the inflation of the inflatable balloon at the treatment site, the flow of blood through the blood vessel is maintained across the treatment site by use of one or more bypass passageways in the medical device.

A catheter and tissue cutting system percutaneously permits the creation of an anastomosis between a first and second anatomical structure, such as a vein and an artery. The system comprises a catheter having a main body with a lumen and tapered distal tip, configured to be moved distally into the first anatomical structure over a primary guidewire. A cutting electrode is nested in the main body, with a lumen which tracks over a secondary guidewire, and is insertable into the secondary anatomical structure. An energy supply is operative to energize the cutting electrode in order to cut a tissue wall defining the first anatomical structure.

A catheter can have a textured outer body surface with protrusions and/or indentations that can reduce friction between the outer body surface and vascular anatomy or an inner lumen of another catheter in contact with the outer body surface. The catheter can include protrusions and/or indentations on an inner lumen surface that can reduce friction between the inner lumen surface and an outer body surface of another catheter within the example catheter. The protrusions can be filled with a lubricant or vasodilating drug, and the protrusions can be configured to break to release the fluid in response to forces on the protrusion during navigation through vascular anatomy and/or an inner lumen of another catheter. The catheter can include a metallic tubular reinforcing layer with openings through which the protrusions and/or indentations extend and/or protrusions and/or indentations shaped into the reinforcing layer.