The invention provides an intermittent catheter comprising a hollow polymeric tubular body comprising a base polymer and a layer comprising a lubricious additive on or comprising a surface of the body, wherein the lubricious additive comprises an amphiphilic molecule.

A medicine powder delivery device and a medicine bottle thereof and a bottle cap of the medicine bottle are disclosed. The medicine powder delivery device includes a medicine bottle and a gas supply member. The medicine bottle has a bottle body and a bottle cap. The bottle body is filled with a medicine powder. When the bottle body is inverted, the bottle body has an unfilled space that is not filled with the medicine powder. The bottle cap includes a cap body, a medicine delivery tube, and a gas delivery tube. The cap body covers the bottle body. The medicine delivery tube and the gas delivery tube extends into the cap body. The medicine delivery tube communicating with the bottle body the gas delivery tube inserted into the unfilled space of the bottle body. The gas supply member is connected to the gas delivery tube.

An introducer sheath for the insertion of a medical device into a blood vessel having an expandable sheath. The sheath has a length, a thickness, and proximal and distal ends. The expandable sheath has a frame extending longitudinally between the proximal and the distal ends, and having an exterior surface and an interior surface that forms an interior lumen along the length of the frame. The frame is configured to achieve an expanded state and a contracted state, the expanded state forming an expanded cross-section in the lumen for passing a medical device therethrough. The frame has a smooth coating about the exterior surface and protrusions extending into the lumen along the interior surface. The introducer sheath can be introduced into a patient in the contracted state, with the distal end of the introducer sheath prevented from moving in the proximal direction by an abutment against a dilator end surface.

An apparatus and methods for tissue restoration are provided. The apparatus may include a catheter shaft extending from a proximal end to a distal tip, the catheter shaft defining lumens including an inflation lumen and a light fiber lumen, a coated balloon positioned on a translucent distal segment of the catheter shaft proximal to the distal tip in fluid communication with the inflation lumen, the coated distal balloon comprising a translucent material and a coated material on an outer surface of the coated balloon, and a light fiber positioned in the catheter shaft in the light fiber lumen and extending through the translucent distal segment.

To reinforce a layer that is configured to contain fluororesin while suppressing the thickness of the entire medical tube. A medical tube includes a first resin layer that is configured to contain fluororesin, and a second resin layer that is configured to coat an outer peripheral surface of the first resin layer and containing polyimide resin. The thickness of the second resin layer is larger than 0 μm but not exceeding 15 μm.

A dilator includes: a hollow shaft having a tapered portion whose outer diameter of the distal end is smaller than the outer diameter of the proximal end; a distal tip, whose proximal end is located at the distal end of the tapered portion, and which is provided to extend toward the distal end direction; and a spirally-arranged protruding portion provided on at least the outer peripheral surface of the tapered portion. The spirally-arranged protruding portion is formed by winding a wire and has gaps between portions adjacent to each other along the longitudinal direction of the hollow shaft. The inner peripheral radius CIDmin of a portion, which is the minimum inner peripheral radius of the spirally-arranged protruding portion, is smaller than the outer peripheral radius TODmax of a portion, which is the maximum outer peripheral radius of the distal tip.

An intravascular treatment system including an introducer sheath having an intentional friction zone along a section thereof imposing an intentional friction force on the outer surface of a catheter shaft slidable therein. The friction zone representing a non-straight (e.g., curved or bent) section of the introducer sheath and/or a section of the introducer sheath whose inner wall has a reduced inner diameter (e.g., fused heat shrink material). During intravascular treatment, sufficient axial force may be applied to overcome the imposed intentional friction force and advance the intravascular treatment device in a distal direction to a desired target site in the artery. Once properly positioned, the imposed intentional friction force ensures that the intravascular treatment device is maintained in place.

A system for disinfecting a medical device is disclosed that includes an elongate instrument comprising a plurality of optical fibers extending along a length of the instrument to a disinfection zone, and a light source coupled with the instrument configured to propagate light distally along the optical fibers. The elongate instrument can be configured to redirect the light radially outward from the instrument. An elongate instrument for disinfecting a medical device can include a plurality of optical fibers extending along a length of the instrument from a proximal end to a disinfection zone at a distal end, the optical fibers configured to propagate a light along the instrument. One or more reflective surfaces can be located within the disinfection zone, and the reflective surfaces can be configured to direct the light radially outward from the instrument.

Devices and methods for the treatment of chronic total occlusions are provided. One disclosed embodiment comprises a method of facilitating treatment via a vascular wall defining a vascular lumen containing an occlusion therein. The method includes inserting an intramural crossing device into the vascular lumen, positioning at least the distal tip of the crossing device in the vascular wall, advancing an orienting device over the crossing device such that an orienting element of the orienting device resides in the vascular wall, inserting a reentry device, and re-entering the true vascular lumen.

A method of performing a medical procedure in a cerebral vessel of a patient including advancing a first catheter system towards an embolus within a cerebral blood vessel and a second catheter system towards the embolus through the first catheter, applying aspiration pressure through the lumen of the second catheter; anchoring a distal end of the second catheter onto the embolus via the aspiration pressure; applying a proximally-directed force on the second catheter; and advancing the first catheter over the second catheter towards the embolus while the distal end of the second catheter remains anchored onto the embolus; and automatically applying aspiration pressure within the first catheter upon the second catheter portion entering into the first catheter.