A guidewire formed from a superelastic material has a proximal section and a distal section. In order to improve torque and pushability in the proximal section, a first wire is wound clockwise onto the proximal section to form a first coil and a second wire is wound counterclockwise onto the first coil to form a second coil.

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 invention provides design, material, manufacturing method, and use alternatives for medical devices. An example medical device includes an elongate shaft having a distal region and a coil disposed along the distal region. The coil is formed from a winding member having a first filar region and a second filar region. The winding member has a first cross-sectional diameter along the first filar region, a second cross-sectional diameter different from the first cross-sectional diameter along the second filar region, a first centroid at a first position along the first filar region and a second centroid at a second position along the second filar region. The first centroid and the second centroid are axially-aligned.

A wire for a medical device includes a wire body and a solid lubrication film. The wire body has an outer circumferential layer formed of a plurality of metal strands that are twisted with each other. The solid lubrication film is formed at least on outside exposed surfaces of the plurality of metal strands. When a virtual circle as a smallest circle enclosing the outer circumferential layer is assumed in a cross section perpendicular to a central axis of the wire body, a part of an outer edge of the solid lubrication film of the cross section is inside the virtual circle and a cross-sectional area of the solid lubrication film in the cross section satisfies A/B>0.7 where A is a size of a portion outside the virtual circle and B is a size of a portion inside the virtual circle.

The invention provides design, material, manufacturing method, and use alternatives for medical devices. An example medical device includes an elongate shaft having a distal region and a coil disposed along the distal region. The coil is formed from a winding member having a first filar region and a second filar region. The winding member has a first cross-sectional diameter along the first filar region, a second cross-sectional diameter different from the first cross-sectional diameter along the second filar region, a first centroid at a first position along the first filar region and a second centroid at a second position along the second filar region. The first centroid and the second centroid are axially-aligned.

Disclosed is an intraluminal catheter that includes a flexible elongate shaft configured to be positioned within a body lumen of a patient, and an intraluminal sensor disposed at the distal portion of the shaft that is configured to sense a characteristic within the body lumen. The shaft further comprises a plurality of wires disposed around a lumen, wherein the wires are helically twisted. The wires can be helically twisted in a single direction to form a cylindrical shape. This helical structure is configured to stiffen the flexible elongate shaft for movement into an obstruction within the body lumen without kinking.

Vascular access kit comprising a guidewire and a needle. The guidewire includes elastic core member ending with guidewire tip segment. Guidewire tip segment comprising widening, guidewire tip rear portion extending distally to the widening, and guidewire tip front portion extending distally from the widening. The needle comprising a beveled opening greater in length than guidewire tip front portion. Guidewire tip rear portion includes a flexing portion configured for causing localized buckling and/or bending for inclining guidewire tip front portion relative to guidewire tip rear portion, in needle beveled opening, when the core member is axially compressed.

The present disclosure describes delivery cables for delivering a medical device. In one embodiment, a delivery cable includes a flexible inner core, a proximal outer coil, and a distal outer coil. The proximal outer coil has a first rigidity. The distal outer coil surrounds at least a portion of a distal section of the flexible inner core and has a second rigidity less than the first rigidity thereby, thereby reducing bias placed on the medical device by the delivery cable.

Provided is a guide wire having a novel structure, with which it is possible to improve production efficiency and to effectively prevent large irregularities from forming on an outer circumferential surface of a core wire. Further provided is a guide wire having a novel structure, with which it is possible to more meticulously set bending rigidity to a distal end portion thereof. In a guide wire having a coil externally mounted about a distal end portion of a core wire, a proximal end portion of the coil is integrally joined to the core wire during formation of the coil. Furthermore, in a guide wire having a coil externally mounted about a distal end portion of a core wire, a cross-sectional shape of a wire that constitutes the coil varies in a lengthwise direction of the coil.

A guide wire includes a first core shaft, a second core shaft, and a covering portion. The second core shaft is made of a material more susceptible to plastic deformation than a material of the first core shaft, and has a proximal end side joined to a distal end side of the first core shaft. The covering portion covers (i) a joint part between the first and second core shafts, and (ii) at least a part of the second core shaft on a distal end side of the joint part. The guide wire includes a first region where the second core shaft on a distal end side of the joint part is covered by the covering portion, and a second region adjacent to the first region, where the joint part is covered by the covering portion. The first region is more susceptible to plastic deformation than the second region.