A medical device comprising a corewire, sensor core, and coupler is presented. A portion of the corewire is disposed within a first end of the coupler, and a portion of the sensor core is disposed within a second end. Alternatively, the device comprises a corewire and a sensor assembly comprising a sensor core having first and second ends and a bore in the first end. A portion of the corewire is disposed within the bore. A method of manufacture comprises providing a corewire, sensor core, and coupler. The method further comprises inserting a portion of the corewire into a first end of the coupler, and a portion of the sensor core into a second end. Alternatively, the method comprises providing a sensor core having first and second ends, and a corewire. The method further comprises forming a bore in the first end, and inserting the corewire into the bore.

A male coupler for a guidewire, the guidewire having a hollow walled tube, the male coupler comprising a connector section, coupled with the guidewire, a portion of the connector section having a diameter smaller than the diameter of the hollow tube, at least one conducting ring coupled with the connector section where the diameter of the connector section is smaller the diameter of the guidewire, wherein the diameter of connector section and the at least one conducting ring substantially equals the diameter of the guidewire.

A steerable guide wire and/or a catheter device and associated method. The device includes a guide wire having a distal end, a hollow interior, and an anchoring mechanism positioned proximate to the distal end of the guide wire. The device further includes a core wire is slidably inserted into the hollow interior of the guide wire. Upon insertion, the core wire actuates the anchoring mechanism to anchor the guide wire at an anchoring location

An apparatus includes a cannula and a grip portion. The cannula includes a first lumen extending from a proximal end to a distal end of the cannula. The grip portion is secured to the proximal end of the cannula. The grip portion includes a second lumen, a transversely oriented vent port, a suction port, and a guidewire port. The second lumen is in communication with the first lumen. The transversely oriented vent port is configured to communicate with the second lumen to thereby vent the second lumen to atmosphere. The suction port is configured to communicate with the second lumen to thereby communicate suction to the distal end of the cannula via the first lumen. The guidewire port is configured to receive a guidewire. The guidewire port is further configured to communicate with the second lumen to thereby provide a path for the guidewire to reach the first lumen.

A device is configured for closing an aperture in a wall of a blood vessel. An embodiment of the device includes a body and at least one suture element held within the body. A suture capture rod is positioned within the body and is operatively associated with the suture element and arranged to pass the suture element through a vessel wall such that opposed portions of the suture element extend from the vessel wall. A removable guidewire segment is removably attached to a distal end of the body.

A guidewire having a first end and a second end, and comprising two or more guidewire modules. Each guidewire module has a first end and a second end. Each guidewire module is configured to be attachable to a second guidewire module by at least one of: attaching the first end of the guidewire module with the second end of the second guidewire module, and attaching the second end of the guidewire module with the first end of the second guidewire module.

A guidewire introducable into a bodily lumen having an obstruction therein is provided. An introducer needle is advanced through tissue and into the bodily lumen. A guidewire is advanced through the introducer and into the lumen. The guidewire is advanced further through the lumen until an atraumatic distal tip of the guidewire encounters an obstruction the distal tip cannot pass in a straight forward manner. The distal tip is pressed against the obstruction such that a flexible segment proximal of the distal tip forms a loop distal of the distal tip. The guidewire is advanced further through the lumen such that the loop of the flexible segment is pushed past the obstruction and the distal tip is pulled distally past the obstruction. A greater diameter guidewire extension can be coupled to the back end of the guidewire, providing function as a larger diameter guidewire.

A guide wire includes a long flexible wire main body, and a coil that is formed by winding a plurality of wires in a spiral shape, and which is disposed at an outer periphery of a distal portion of the wire main body to cover the distal portion. The coil includes a coil distal portion that is disposed on a distal side in the distal portion, a coil proximal portion that is disposed on a further proximal side in comparison to the coil distal portion, and a coil intermediate portion that is disposed between the coil distal portion and the coil proximal portion, and includes a wire having a wire diameter that is smaller than a wire diameter of the wires of the coil distal portion and the coil proximal portion.

The present disclosure relates to the field of endovascular treatment. More particularly, the present invention is a disc balloon which is designed to implement safer endovascular treatments, primarily by allowing many middle cerebral artery aneurysms that are currently clipped to be treated with coiling.

A short length flexible catheter with hollow guide wire and flushing port for convection enhanced delivery may be provided. The short length CED catheter may include a catheter body made of silicone or plastic. The short length catheter may further include an attachment port connected to a first end of the flexible, hollow guide wire contained within the catheter body. The hollow catheter guide wire may extend beyond the catheter body on one end for both enhanced tunneling and simultaneous use of flushing.