Intraluminal and endovascular devices and methods of manufacturing intraluminal and endovascular devices may be provided. In one implementation, an intraluminal device may include a sheath having a flexible distal bending segment and a core wire arranged within the sheath. The core wire may include a distal end portion doubled back in a loop within the sheath such that the distal tip of the core wire is situated proximally from the loop. The intraluminal device may also include a movement restrictor within the sheath that is configured to limit axial movement of the distal tip of the core wire. Limiting the axial movement of the core wire distal tip may cause the loop of the core wire to buckle, resulting in a bend in the distal bending segment of the sheath, when a force is exerted on the core wire.

The current document is directed to usable-length-selectable catheters that employ usable-length-selectable catheters to treat malformations, constrictions, obstructions, lesions, and blockages within patients' blood vessels. The usable length of the shaft of a usable-length-selectable catheter, to which the current application is directed, can be adjusted over a set of lengths prior to and during medical procedures.

The embodiments presented herein relate to concepts designed to eliminate the gap between a catheter and guide wire that can otherwise contribute to a catheter getting stuck within the vasculature.

A device and its method of use eliminates or reduces the gap between a catheter and guide wire that can otherwise contribute to a catheter getting stuck within the vasculature. The device is maintained at or near the distal end of the catheter while being advanced through the vessels of a patient. The reduced gap size prevents the catheter from otherwise catching on various structures of a vessel, such as a bifurcation.

There is described a tip shaping device for shaping a tip of a guidewire, including an elongated body extending along a longitudinal axis between two end faces and having a lateral face extending along the longitudinal axis between the two end faces; and a planar body projecting from the lateral face of the elongated body, the planar body including a flexible section located adjacent to the elongated body and wrappable around at least a portion of the lateral face of the elongated body, the planar body having a guidewire receiving face adapted to shape the guidewire when received thereon and upon rotation of the elongated body over the planar body.

A non-vascular lumen guide wire, comprising a mandrel (1) and a ball head (2) prepared with a metal material, wherein an outer diameter of the insertion end of the mandrel (1) is smaller than the outer diameter of the non-insertion end of the mandrel; the insertion end of the mandrel (1) is connected to the ball head (2), a plastic coating layer (3) is wrapped around the outer side of the mandrel (1), the outer diameter of the ball head (2) is larger than the outer diameter of the insertion end of the plastic coating layer (3), and the outer diameter of the ball head (2) is not larger than the non-insertion end of the plastic coating layer (3). The guide wire, by means of using a ball head (2) with a diameter slightly larger than the plastic coating layer (3) at a far end, may effectively avoid the defects that the guide wire falls off in actual use, or the plastic coating layer (3) at the far end easily rolls up when inserted. The ball head (2) is made of metal material, has a relatively large outer diameter, and has great visibility under an endoscope and an X-ray. A doctor may clearly observe a puncture area reached by the tip end of the guide wire, and the effect of avoiding a guide wire end from puncturing an inner wall of lumens may be realized without the need for a positioning device.

A guidewire including a thin elongated structure and an outer shell around at least a portion of the thin elongated structure. The outer shell includes a first portion and a second portion. The first portion and the second portion of the outer shell are each coupled to the thin elongated structure. The first portion is spaced from the second portion by a gap. The guidewire is configured to move between a flexible state and a rigid state. The gap has a first distance when the guidewire is in the flexible state and the gap has a second distance greater than the first distance when the guidewire is in the rigid state.

A system a guidewire and a tensioning mechanism. The guidewire includes a thin elongated structure and an outer shell around a first portion of the thin elongated structure. A second portion of the thin elongated structure is exposed outside the thin elongated structure. The tensioning mechanism is configured to engage the second portion of the thin elongated structure to move the guidewire between a flexible state and a rigid state.

The current document is directed to usable-length-selectable catheters that employ usable-length-selectable catheters to treat malformations, constrictions, obstructions, lesions, and blockages within patients' blood vessels. The usable length of the shaft of a usable-length-selectable catheter, to which the current application is directed, can be adjusted over a set of lengths prior to and during medical procedures.

A guidewire including a thin elongated structure and an outer shell around at least a portion of the thin elongated structure. The outer shell includes a first portion and a second portion. The first portion and the second portion of the outer shell are each coupled to the thin elongated structure. The first portion is spaced from the second portion by a gap. The guidewire is configured to move between a flexible state and a rigid state. The gap has a first distance when the guidewire is in the flexible state and the gap has a second distance greater than the first distance when the guidewire is in the rigid state.