Abstract: An actuating member for causing a flexible elongated member for medical use to perform a predetermined curving motion includes a push-pull member including a first moving part and a second moving part which are configured to be movable relative to one another in an axial direction of the elongated member, the first moving part and the second moving part being pushable and pullable so as to cause the elongated member to curve in the axial direction of the elongated member; a curving motion restricting member which is configured to be movable in the axial direction of the elongated member, and which is configured to restrict curving of at least a portion of the elongated member; and an operation member configured to operate movements of the first moving part, the second moving part, and the curving motion restricting member.

Abstract: A method for bringing an IVUS and an OCT image into register. In one embodiment, the method includes obtaining an IVUS image of an area of a lumen; obtaining an OCT image of the same area of the lumen; determining the same asymmetry in each of the IVUS and OCT images; and overlaying the IVUS and OCT images and rotating them with respect to one another until the asymmetry in each of the IVUS and OCT images are in register, and determining the angle of rotation that resulted in the registration. In another aspect, the invention relates to a probe for OCT and IVUS imaging. In one embodiment, the probe includes a sheath having a first end and a second end defining a lumen; a marker that is opaque to light and ultrasound located between the first end and second end; and an IVUS/OCT probe head positioned within the sheath.

Abstract: A catheter assembly including a tapered steering spine having a varying stiffness along an axial length. The tapered steering spine is tailored to provide increasing flexibility from proximal to distal in a way that makes the bend radius more uniform along the length of the steering section. In one embodiment, the tapered steering spine includes structures on adjacent rings that engage with each other when the steering section is flexed to limit the minimum bend radius to a predetermined minimum and which enhances the torsional rigidity of the steering section regardless of the degree of flexure of the steering section. The limited bend radius can prevent excessive bending of components such as fiber optics. The enhanced torsional rigidity can negate the need for torque braid in the section of the catheter shaft that surrounds the tapered steering spine.

Abstract: A steerable laser probe may include a handle, and inner bore of the handle, an actuation lever of the handle, a housing tube, and an optic fiber disposed within the inner bore of the handle and the housing tube. The housing tube may have a first housing tube portion having a first stiffness and a second housing tube portion having a second stiffness. The second stiffness may be greater than the first stiffness.

Abstract: Devices for and methods that can be used in endoscopic surgery, and more particularly, devices and methods that can be used for endoscopically applying surgical sealants and other fluids to internal organs and tissues.

Abstract: Disclosed is a pericardiocentesis needle component (10), comprising a guide wire (13) and a puncture needle (12). The guide wire (13) extends into and through the puncture needle (12), and the guide wire (13) comprises a bent section (32) at the distal end and a straight section at the proximal end. The bent section (32) at the distal end is formed by bending the guide wire (13), and the end of the bent section is a pointed-shape structure. The guide wire (13) is made of a highly elastic material. The pointed end rotates at least 90 degrees within a range of no more than 3 mm starting from the pointed end at the bent section (32) of the guide wire. The pericardiocentesis needle component (10) of the present invention is less likely to damage a heart during a pericardiocentesis procedure.

Abstract: A steering handle for a catheter. The steering handle includes a thumb knob arrangement for driving a cam assembly that in turn actuates a pull wire or pull wires. In some embodiments, the cam assembly includes a set of dual pins that actuate the pull wire in a quasi-linear relationship between cam rotation and axial displacement of the wire. In certain embodiments, the second set of dual pins imparts a reverse action on a second pull wire, also in quasi-linear fashion. That is, when one wire is released by the cam assembly, the other wire is taken in by the cam assembly. In various embodiments, the quasi-linear action can cause release of more pull wire than is taken in, thereby helping prevent the released pull wire to act as an unwanted counter force to the actuated pull wire.

Abstract: An interventional catheter is adapted for treating a blood vessel. In an embodiment, the catheter includes an elongate shaft sized for insertion in a blood vessel and a stent positioned on a distal region of the elongate shaft. An expandable dilation member is coupled to a distal region of the elongate shaft. The expandable dilation member is adapted to expand outward. A stent containment member is positioned over the elongate shaft and the stent to contain the stent in a collapsed state.

Abstract: An infusion flow guidewire and a system including an infusion flow guidewire. The minimal cross section flexible infusion flow guidewire includes a nitinol hypotube, a flexible tip having a closed distal end, a coil, a core wire and at least one distally located rearwardly directed jet orifice for infusion of fibrinolytics and for introduction of high pressure fluids for maceration and rearwardly directed flow of thrombus debris located in tortuous small sized vessels. Apparatus, some of which is removably attachable, is provided in the system for grasping members of the invention for rotational torqueing and for longitudinal actuation along and within the vasculature.

Abstract: A catheter assembly for use in accessing a vasculature of a patient is disclosed. In one embodiment, the catheter assembly includes a catheter body that includes a flattened oval outer surface and defines first and second lumens. The catheter body defines a distal tip region that includes a venous lateral opening that is in fluid communication with the first lumen and includes a distal-facing portion. The distal tip region further includes an arterial lateral opening that is in fluid communication with the second lumen, includes a distal-facing portion, and is substantially un-staggered with respect to the venous lateral opening. A distal end opening is in fluid communication with a power injectable third lumen. In another embodiment, the first and second lumens each generally include a reniform cross-sectional shape. In yet another embodiment, a dual-lumen catheter includes first and second lumens that each define a modified ellipse cross-sectional shape.

Abstract: Weight loss can be promoted by introducing a microcatheter into the mid segment or distal portion of a human subject's left gastric artery and delivering, via the microcatheter, a plurality of particles with sizes between 300 and 500 ?m into the distal portion of the subject's left gastric artery. The particles cause endovascular flow reduction or interruption in the distal portion of the subject's left gastric artery. The reduced or interrupted blood flow decreases the production of the hormone ghrelin, which reduces the subject's appetite, thereby promoting weight loss.

Abstract: An atherectomy catheter has a shaft having an opening in the side wall, a cutter which is positioned near the opening in the internal space of the shaft and which can move in the axial direction of the shaft, and a distal end portion connected to the distal end of the shaft. The distal end portion has a blade tube connected to the distal end of the shaft by continuing the internal space, a reduced diameter portion connected to the distal end of the blade tube by continuing the internal space, and a distal end tip whose outer diameter is smaller than the outer diameter of the distal end of the blade tube, whose distal end side is projected outward from the distal end of the reduced diameter portion, and whose proximal end side is extended into the internal space of the blade tube through the internal space of the reduced diameter portion.

Abstract: A delivery device for a collapsible prosthetic heart valve may include an operating handle and a catheter assembly. The handle may include a housing, a piston cylinder, a piston longitudinally slidable within the piston cylinder, the piston and the piston cylinder together defining at least one pressure chamber, a deployment actuator coupled to the housing and rotatable relative thereto, and a pneumatic switch adapted to provide a pressurized fluid to the pressure chamber to apply a longitudinal force to the piston. The catheter assembly may include a first shaft around which a valve-receiving compartment is defined, the first shaft being operatively connected to the housing, and a distal sheath operatively connected to the piston, the distal sheath being moveable between a closed condition covering the compartment and an open condition uncovering the compartment. Longitudinal movement of the piston may move the distal sheath between the closed and open conditions.

Abstract: A guidewire insertion aid is is configured to feed out a guidewire inserted in a housing in order to insert said guidewire into the lumen of a piece of medical equipment. In some examples, the insertion aid comprises: a main body, a housing support part and a guidewire support part. A sliding contact part is disposed between the housing support part and the guidewire support part. The sliding contact part extends in the lengthwise direction of the main body and has a sliding contact surface for the guidewire. A feed-out member is provided on the main body and has a water-retentive water-retention member. The feed-out member is disposed with the water-retention member side thereof facing towards the sliding contact surface. The feed-out member can be displaced while the guidewire is held between said feed-out member and the sliding contact part.

Abstract: A rotatable thrombectomy wire for breaking up thrombus or other obstructive material comprising an inner core composed of a flexible material and an outer wire surrounding at least a portion of the inner core. The outer wire has a sinuous shaped portion at a distal region. The inner core limits the compressibility of the outer wire. The outer wire is operatively connectable at a proximal end to a motor for rotating the wire to macerate thrombus.

Abstract: A recanalization catheter for facilitating re-entry into a lumen of a blood vessel from a subintimal space. The recanalization catheter includes first and second mechanically actuatable wings positioned at a distal region of the elongate shaft of the catheter that are actuatable between a retracted position and an expanded position. In the retracted position the mechanically actuatable wings are positioned in first and second elongate channels defined in the elongate shaft, and in the expanded position the mechanically actuatable wings extend outward from the first and second elongate channels. The actuatable wings extend in an arcuate path away from the elongate shaft in the expanded position to be positionable in a circumferential orientation within a subintimal space formed in a vessel wall to automatically orient a lateral port of the elongate shaft toward the true lumen.

Abstract: An introducer sheath includes a tubular body portion having a proximal region and a distal region, and defines an internal lumen configured and dimensioned to slidably receive a catheter. A penetrating portion at a distal end of the tubular body has a first tapered configuration to enlarge an opening in a body tissue during distal advancement of the introducer sheath through the body tissue and a second expanded configuration to enable the passage of a distal end portion of a catheter through the penetrating portion.

Abstract: A method and apparatus providing precision external control of interventional medical procedures is presented. The apparatus includes a fixed frame, the fixed frame attachable to a patient and to a secure structure. The apparatus also includes a precision actuator in mechanical communication with the fixed frame, the actuator directing motion of a wire within a catheter or a catheter within the patient. Additionally the apparatus includes a control device in electrical communication with the actuator, wherein the control device controls the actuator.

Abstract: A vascular nerve ablation (denervation) system includes a multiplicity of expandable needles which open around a central axis to engage the wall of a blood vessel allowing the injection of a cytotoxic or neurotoxic solution for ablating conducting tissue in and near the vessel wall of a renal artery or pulmonary vein. The expandable needles are formed of self-expanding materials and include structures which limit the distance of penetration of the injection needles into the tissue of the wall of the blood vessel.

Abstract: Catheter including an inner tubular member having a fluid lumen defined therein and an exterior surface. The exterior surface defining a first distal flow port and a second distal flow port. An outer tubular member is movable relative to the inner tubular member in a proximal direction and having an interior surface. A first pressure chamber is defined between the exterior surface and the interior surface, and between a first distal seal assembly and a first proximal seal assembly. A second pressure chamber is defined between the exterior surface and the interior surface, and between a second distal seal assembly and a second proximal seal assembly. Fluid introduced through the fluid lumen pressurizes the first pressure chamber and the second pressure chamber to generate a respective force at the first proximal seal assembly and to the second proximal seal assembly to urge the outer tubular member in the proximal direction.

Abstract: True lumen reentry devices and methods useable for redirecting a guidewire from a subintimal tract within a wall of a blood vessel into the true lumen of the blood vessel. A reentry catheter device comprises a main catheter shaft having at least one guidewire outlet aperture with at least one side tube located on a distal portion of the main catheter shaft. The side tube(s) is/are tracked over initially inserted guidewire(s) to advance a distal portion of the reentry catheter device into the subintimal tract with a guidewire.

Abstract: An object removal tool including a basket device having a basket section; a sheath on the basket device, where the sheath is adapted to longitudinally slide on the basket device; and a control connected to the basket device and the sheath. The control is configured to longitudinally move the sheath on the basket device to close the basket section on an object.

Abstract: A medical device and method for manipulating movement of a micro-catheter, the device comprising an elongated tubular member having at least one lumen therein, wherein the lumen is proximally coupled to a pressurized fluid control system configured to regulate fluid flow through the elongated tubular member. An aperture is disposed near a distal end of the elongated tubular member, the aperture being in fluid communication with the at least one lumen. In one aspect, the aperture is oriented at an angle which is non parallel to the longitudinal axis of the elongated tubular member. A nozzle is coupled to the aperture, wherein the nozzle is configured to regulate pressurized flow out of the catheter to manipulate movement of the distal end of the elongated tubular member.

Abstract: Vascular dilator systems, kits, and methods allowing for sheathless introduction of a treatment device into a body vessel or body cavity are disclosed. A vascular dilator system can include a dilator assembly, including a tubular shaft and a deformable member, and optionally, the treatment device. The deformable member can include a non-biodegradable material and can have a diameter at a proximal end portion that is greater than a diameter at a distal end portion. The distal end portion of the deformable member can be coupled to an outer surface of the tubular shaft, at or near a shaft distal end portion. The proximal end portion of the deformable member can include a diameter configured to receive or stretch around a distal end portion of the treatment device. In use, the deformable member can provide a tapered bridge between the outer surface of the tubular shaft and an outer surface of the treatment device.

Abstract: A catheter has a distal assembly with at least one loop, if not two, with ring electrodes. The distal assembly has an elongated support member covered by an extruded form having two lumens, one sized for nonslip tight fit with the support member. A single continuous puller wire for bidirectional deflection is pre-bent into two long portions and a U-shape bend therebetween. The U-shape bend is anchored at a distal end of a deflectable section which is reinforced by at least one washer having at least two holes, each hole axially aligned with a respective lumen in the deflectable section. Each hole is centered with a lumen so that each puller wire portion therethrough is straight and subjected to tensile force only. A proximal end of the support member is flattened and serrated to provide a better bonding to the distal end of the deflectable section.

Abstract: A catheter assembly having first and second shaft members that provide stearability for the catheter assembly. The first shaft member has a plurality of longitudinally spaced apart first ring members that are interconnected with a longitudinally extended first spine member. The second shaft member is positioned within the first shaft member and is connected to a distal end portion of the first shaft member. The second shaft member has a plurality of longitudinally spaced apart second ring members that are interconnected with a longitudinally extending second spine member. Alternatively, the second shaft member includes a plurality of protrusions extending radially outward from the longitudinally extending second spine member. The second shaft member is operable to move at least portions of the first ring members longitudinally relative to each other to bend the first shaft member.

Abstract: A catheter loading device includes a guidewire section, a catheter section, and a hinge that connects a proximal end of the guidewire section to a distal end of the catheter section. The guidewire section is rotatable relative to the catheter section about a rotation axis between a first position and a second position. When the guidewire section is in the first position, a longitudinal axis of a guidewire positioned in a channel of the guidewire section is aligned with a longitudinal axis of a lumen of a catheter positioned in a receiver of the catheter section. When the guidewire section is in the second position, the longitudinal axis of the guidewire positioned in the channel is not aligned with the longitudinal axis of the lumen of the catheter positioned in the receiver.

Abstract: A system and method for treating a patient including advancing a catheter into the vasculature of the patient, forcing the catheter to adopt a position in contact with a vessel wall, and causing a needle tip to advance into the wall from a lumen in the catheter external surface that is in contact with the wall.

Abstract: A catheter apparatus may have a flexible shaft, guidewire lumens passing through the shaft, and a positioning device for positioning the guidewires relative to an external lumen. The positioning device may be an expansible scaffold covered with a retractable sheath. The positioning device may also be one or more balloons that are inflated through an inflation port in the shaft. The catheter apparatus may be operated by inserting a guide catheter into a vasculature with a chronic total occlusion, inserting the catheter apparatus into the guide catheter, and advancing the guidewires through the guidewire lumens and into contact with a chronic total occlusion. The positioning device may be activated before and/or between attempts to pass the guidewires through the chronic total occlusion to interrogate various parts of the chronic total occlusion.

Abstract: Embodiments of a method and apparatus to prevent reperfusion injury. In one embodiment, blood flow proximal to a lesion is occluded. An infusion catheter is advanced to a region distal to the lesion and an anti-reperfusion injury drug is delivered. The lesion may then be treated with a dilating device to reintroduce blood flow to the region distal to the lesion.

Abstract: A guide wire has excellent flexibility of a distal portion thereof, followability for a blood vessel and the like and transmutability of delicate interactions such as resistance produced when the distal portion slides in contact with a wall surface of a blood vessel and the like, and resistance produced when the distal portion bumps against a stenosed section and the like. The guide wire has a core shaft and a coil body covering a distal portion of the core shaft, the coil body being formed by helically winding a stranded wire having three or more elemental wires interwound together, and the stranded wire being hollow and having a first void at the center thereof.

Abstract: A catheter advancement device includes a housing with a catheter inlet, a catheter outlet, and a manually actuated finger drive mechanism. The drive mechanism frictionally engages a catheter inserted into the inlet and advances the catheter through the housing and into or out of another device, such as a needle. The housing may be slidable along the needle.

Abstract: A steerable medical device is used to controllably introduce a guidewire or other medical instrument into a body of a patient and direct placement of the guidewire or other medical instrument in the body of the patient. The steerable medical device can include an elongated member, a steering mechanism, and an attachment member. The elongated member extends along a longitudinal axis and comprises a deflectable distal portion that is deflectable off of the longitudinal axis. The steering mechanism is adapted to control longitudinal and rotational movement of the elongated member and to control off-axis deflection of its deflectable portion. The attachment member is removably couplable to another medical device. The attachment member is moveably coupled to the steering mechanism and the elongated member.

Abstract: A catheter adapted for ablation, mapping, injection, and directional control by an external magnetic system has a catheter body, an intermediate section, and a tip section having a tip electrode configured with an omnidirectional distal end and a concentric needle port. The tip electrode houses a magnetic device and a position sensor arranged in an integrated configuration, wherein the configuration facilitates a path in the tip section for a component, including an injection needle, to extend through the tip section for extension and retraction with reduced stress and friction. The integrated configuration is an efficient use of space in the tip electrode that allows the tip section to carry both the position sensor for determining location and orientation of the tip section and the necessary volume of magnetic or magnetizable material to accomplish magnetic navigation.

Abstract: It is intended to provide a thrombus-aspiration catheter capable of exerting flexibility and aspiration force even in the case where the tube in the front end side is a triple lumen tube or a contrast marker is provided at the front end. A thrombus-aspiration catheter (1) comprising a basal end side tube (2) of the double lumen type which has an aspiration lumen (11) and a core wire lumen (12), and a front end side tube (3) of the triple lumen type which has a guide wire lumen (13) in addition to the aspiration lumen (11) and the core wire lumen (12), wherein the front end of the above-described front end side tube is obliquely cut and a terminal aspiration tube (4) of a flexible double lumen, which has a front end opening (41) inclined in almost the same direction as the cut face (31), is connected to the cut face.

Abstract: In one instance, a catheter for replacing or adding a guide wire into a patient is provided. The catheter includes a first rapid exchange lumen, a second rapid exchange lumen, and a releasable wire-securing device. A second guide wire is placed in the second rapid exchange lumen and secured into position. The catheter is then advanced along the first guide wire until in position, and then the second guide wire is released from the wire-securing device and advanced into the desired position. The catheter is then removed. Other catheters and methods are also disclosed.

Abstract: Systems and methods for accessing body tissue are disclosed. The systems and methods can include an introducer assembly for percutaneous access to a body lumen. The assembly can include a needle and an over-the-needle guidewire. The needle and the guidewire can be inserted into body tissue and the guidewire advanced into the body tissue relative to the needle. The needle can be removed after advancing the guidewire.

Abstract: A Foley catheter assembly is disclosed. The Foley catheter assembly includes a Foley catheter, which includes an insertion tip inserted into the bladder and a drainage tube extending from the insertion tip and draining urine from the bladder, and a catheter support cover, which covers the outer surface of the Foley catheter before insertion of the Foley catheter into the bladder to prevent contamination and allows smooth insertion of the insertion tip into the bladder at a constant speed. The catheter support cover includes a pair of support main bodies that are detachably coupled to each other and accommodate the drainage tube and a pair of transport rollers disposed at both sides of the insertion tip at upper portions of the support main bodies to be rotatable for inserting the insertion tip into the bladder.

Abstract: Systems and methods are disclosed that include a guide catheter apparatus insertable through a external body passage of a subject. The guide catheter apparatus includes a substantially rigid shaft and a handle. The shaft has a proximal opening, a distal opening, and a lumen extending between the proximal opening and the distal opening. The handle has a structure to allow a position of the guide catheter to be controlled by some or all of three fingers of one hand of an operator of the handle. The structure of the handle is adapted to permit the operator to position a thumb and index finger of the hand to manipulate a working device inserted into the lumen of the guide catheter, where the working device is manipulable via a portion of the working device immediately adjacent to the handle.

Abstract: A method and apparatus for manipulating a surgical guidewire. The apparatus comprises a chuck for selectively coupling motive force to a surgical guidewire and an actuator, coupled to the chuck, for imparting an axial motive force to the chuck. Embodiments of the invention further comprise a method of using the apparatus.

Abstract: A medical probe includes a proximal section, a transition region, and a distal section. The proximal section includes a braid that is braided with a cross-braiding configuration. In the transition region, which follows the proximal section, the braid transitions between the cross-braiding configuration and a helical coiling configuration. In the distal section, which follows the transition region, the braid is coiled with the helical coiling configuration.

Abstract: A deflection mechanism for use in an elongate medical device is presented. The deflection mechanism comprises an actuator. The actuator comprises a rotatable body comprising a channel. The deflection mechanism further comprises an activation wire having a proximal end and a distal end, and a wire lock attached to the proximal end of the activation wire. The wire lock is disposed within the channel and is configured to ride therein when the actuator body is rotated. An elongate medical device, and a handle assembly thereof, that incorporate the deflection mechanism are also presented.

Abstract: A medical device handle assembly can include a modular extension that allows for the addition of any number of connector ports to an existing handle. In an embodiment, such an extension can comprise a main body portion configured to be coupled with an elongate medical device shaft comprising at least one of an electrical wire and a fluid lumen. The main body portion may comprise a handle port configured to provide access to one or more of a fluid connector fluidly coupled with the fluid lumen and an electromechanical connector electrically coupled with the electrical wire. The handle assembly can further comprise a handle extension portion coupled with the handle port.

Abstract: A tether holder has a locking portion, for securing a proximal end of a tether, and a pin portion that may fit within a receptacle of a handle assembly of a tool. A distal member of an inner assembly of the tool engages an implantable medical device, from which the tether extends, through at least one lumen of the inner assembly and out through a proximal port of the handle assembly, which is located in proximity to the receptacle. An enlarged distal-most portion of a deployment tube of the tool contains the distal member and the device, and is moveable, relatively to the inner assembly and the device, to deploy the device out through a distal opening of the tool. The handle assembly may also include a flush lumen and a tether engaging conduit, both in fluid communication with the at least one lumen of the inner assembly.

Abstract: A housing tool suppresses rotation of a tubular body in a winding direction that holds an elongated medical body in a packaging body, and suppresses deformation of a distal end portion of the elongated medical body. The housing tool includes a tube-shaped holder that is wound in a circular shape for holding a guide wire, a fastening member that fixes adjacent portions of the wound holder, and a mounting member that includes engagement portions and to be engaged with the fastening member, reaches an outer side of a circle of the holder wound in a circular shape, and covers an end portion of the holder from which the guide wire is derived.

Abstract: A shaft suppresses a rise in operation resistance as it is pushed and pulled even inside an extremely winding blood vessel and thus secures sufficient torque transmission characteristics and operability. A guidewire may employ the above-described shaft. The shaft is twisted along its longitudinal axis and has a cross section that forms a substantially rectangular shape in a direction perpendicular to the longitudinal axis. Moreover, the cross section of the shaft has a projection that projects arcuately.

Abstract: A method of making a core metal element for a medical guidewire comprising providing a wire of nickel titanium alloy having a length that includes a proximal portion having a first diameter and a distal portion having a second diameter. Applying cold work to the distal portion and not applying cold work to the proximal portion, thereby imparting to the distal portion a third diameter that is smaller than the second diameter; and then applying a reducing process to the wire whereby the proximal portion is reduced to have a fourth diameter that is less than the first diameter.

Abstract: A shaft suppresses a permanent set, or plastic deformation, even when inserted into an extremely winding blood vessel. A guidewire incorporates the above shaft. The shaft is twisted along its longitudinal axis and has a cross section forming a substantially rectangular shape extending in a first direction perpendicular to the longitudinal axis. The cross section has at least one arcuate recess.

Abstract: Medical devices and methods for making and using medical devices are disclosed. An example medical device may include a guide extension catheter. The guide extension catheter may include a push member having a proximal portion with a proximal stiffness, a distal portion with a distal stiffness different from the proximal stiffness, and a transition portion disposed between the proximal portion and the distal portion. The transition portion may provide a smooth transition between the proximal stiffness and the distal stiffness. The push member may have a first outer diameter. A distal tubular member may be attached to the push member. The distal tubular member may have a second outer diameter larger than the first outer diameter.

Abstract: A guide wire has a coil body covered with a hydrophilic coating film that exhibits sufficient lubricity even when there is little moisture in its surroundings. In the coil-type guide wire, a coating portion is formed by a plurality of layers where the innermost layer includes a hydrophobic film and an outer layer includes a hydrophilic film. Portions of the innermost layer extend between adjacent coils of the coil body and spaces are formed between the outer layer thereof and the portions of the innermost layer between the coils. The spaces allow moisture to pool so that when moisture in the guide wire's surroundings decreases, it is possible to supply the moisture pooled in the spaces to the hydrophilic film. Thus, even when there is little moisture in the guide wire's surroundings, it is possible to have a sufficient amount of lubricity.