A guide wire includes an elongated wire body having flexibility; a distal member that covers a distal portion of the wire body and is configured to have a resin material; and a hydrophilic lubricant layer that is formed so as to cover a proximal end of the distal member and is configured to have a hydrophilic material. In addition, the hydrophilic lubricant layer has a tapered shape whose outer diameter gradually decreases toward a proximal side. In addition, the maximum outer diameter of the hydrophilic lubricant layer is smaller than the maximum outer diameter of the distal member. In addition, a proximal portion of the distal member has a tapered shape whose outer diameter gradually decreases toward the proximal side, and a distal end of the hydrophilic lubricant layer is positioned at the tapered portion of the distal member.

A venous access catheter is combined with a needle, guidewire, and actuator where the needle is disposed coaxially over the guidewire and the catheter is disposed coaxially over the needle. A hub at a proximal end of the access catheter includes a wiping element to clean blood from the needle and guidewire as they are removed and a side port to allow connection of fluids after the access catheter is placed.

Intravascular devices, systems, and methods are disclosed. In some instances, the intravascular devices are guide wires that include a distal sensing element mounted partially within a housing and embedded and/or surrounded by a flexible adhesive. For example, in some implementations a sensing guide wire includes a flexible elongate member; a housing coupled to the flexible elongate member; a flexible element extending distally from the housing; and a sensing element coupled to the flexible elongate member such that a proximal portion of the sensing element is positioned within the housing and a distal portion of the sensing element is positioned within the flexible element. A flexible adhesive can embed or surround the distal portion of the sensing element positioned within the flexible element. Methods of making, manufacturing, and/or assembling such intravascular devices and associated systems are also provided.

An IV device assembly may include a lumen forming a fluidic channel within the IV device assembly. The lumen may be fluidically coupled to a vascular access device (VAD) coupler via a funnel coupler, and an IV device assembly coupler at a proximal end of the lumen. The IV device assembly may also include one or more of the following: a collapsible sleeve formed coaxially around a first portion of the lumen and mechanically coupled to the funnel coupler, a probe formed along a second portion of the lumen within the collapsible sleeve and into the VAD coupler, a translation handle that translates the probe out of a distal end of the VAD coupler, and a fixed grip formed around the lumen to maintain a position of the IV device assembly relative to the translation handle.

An IV device assembly may include a lumen forming a fluidic channel within the IV device assembly. The lumen may be fluidically coupled to a vascular access device (VAD) coupler via a funnel coupler, and an IV device assembly coupler at a proximal end of the lumen. The IV device assembly may also include one or more of the following: a collapsible sleeve formed coaxially around a first portion of the lumen and mechanically coupled to the funnel coupler, a probe formed along a second portion of the lumen within the collapsible sleeve and into the VAD coupler, a translation handle that translates the probe out of a distal end of the VAD coupler, and a fixed grip formed around the lumen to maintain a position of the IV device assembly relative to the translation handle.

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.

A medical wire includes a first flexible tube that extends in a front-rear direction and is formed to be bendable, an operation wire that extends in a front-rear direction and is inserted into the first flexible tube, and a support that is fixed to a rear end portion of the first flexible tube, in which a front end portion of the operation wire is fixed to a front end portion of the first flexible tube while being separated from a central axis of the first flexible tube in one direction in a radial direction.

An elongated guidewire assembly has a distal segment configured to be selectively maneuvered, along an elongated Introducer assembly. The distal segment is configured to selectively transmit a tenting force from the elongated guidewire assembly to the first biological wall after the distal segment has contacted, at least in part, the first biological wall and the distal segment has been selectively protracted away from the distal introducer assembly.

An intravascular device (1) is configured such that a first end section (1a) is disposed in a blood vessel of an organism, and an electrode for detection or stimulation of nerve tissue located outside the blood vessel is provided to the first end section (1a). The intravascular device (1) includes: an electrically-conductive wire member (10); at least one electrode member (20) that is provided on the first end section (1a) side and that is electrically connected to the wire member (10); and difference reduction sections (30, 40) that reduce a level difference caused by an outer diameter difference between the outer diameter of the electrode member (20) and the outer diameter of the wire member (10). The electrical resistance between the electrode member (20) and a second end section (1b) of the wire member (10), which is on the side opposite from the first end section (1a), is 100 or less.