Abstract: A balloon catheter, and method of making the same, which includes an elongated shaft, and an expandable member affixed to the distal portion of the elongated shaft such that a section of the elongated shaft extends through at least a portion of the expandable member. The elongated shaft includes a radiopaque portion that includes a radiopaque material disposed in a non-metallic coating material. In some embodiments, the radiopaque portion is positioned adjacent the expandable member such that the position of at least a portion of the expandable member (or a stent disposed thereon) can be identified or determined within the vasculature in which it is deployed using an appropriate imaging technique, such as fluoroscopy. Additionally, in some embodiments, the radiopaque portion can define one or more raised areas on the elongated shaft adjacent the expandable member. In such embodiments, the raised area or areas in the radiopaque portion can function as mounting bodies for mounting a stent.

Abstract: An angioplasty catheter and method for making and using the same. An angioplasty catheter comprises an inner tube having a proximal end, a distal end, and a lumen extending therethrough; an outer tube disposed over the inner tube, the outer tube having a proximal end and a distal end; a balloon coupled to the distal end of the outer tube; an inflation lumen defined between the inner tube and the outer tube, the inflation balloon in fluid communication with the balloon; and a support block coupled to the inner tube. In addition, a method for manufacturing an angioplasty catheter is disclosed.

Abstract: A medical device in which a melt processed part has different crystallized properties at different locations. The part is formed of a polymer composition by inclusion a of polymer crystallization modifier in the composition making up at least a portion of such part, the amount of the polymer crystallization modifier is varied at different locations on the part in accordance with the desired difference in crystallization behavior.

Abstract: A medical device in which a melt processed part has different crystallized properties at different locations. The part is formed of a polymer composition by inclusion a of polymer crystallization modifier in the composition making up at least a portion of such part, the amount of the polymer crystallization modifier is varied at different locations on the part in accordance with the desired difference in crystallization behavior.

Abstract: The invention provides small molecule drugs that are chemically modified by covalent attachment of a water-soluble oligomer obtained from a monodisperse or bimodal water-soluble oligomer composition. A conjugate of the invention, when administered by any of a number of administration routes, exhibits a reduced biological membrane crossing rate as compared to the biological membrane crossing rate of the small molecule drug not attached to the water-soluble oligomer.

Abstract: A catheter comprises a first component and a second component. The first component has a first outer diameter and the second component has a second outer diameter. At least a portion of the first component being bonded to at least a portion of the second component. When the at least a portion of the first component is bonded to the at least a portion of the second component the first outer diameter is substantially equal to the second outer diameter. A heat shrink material being utilized to bond the at least a portion of the first component to the at least a portion of the second component.

Abstract: A catheter for delivering a medical device into a body lumen, and method for preparing said catheter, wherein the catheter comprises an elongate body, at least a portion of which defines a medical device retaining region for retaining a medical device thereon. At least a portion of the medical device retaining region comprises a predetermined pattern of material. The predetermined pattern of material is a photoresist material that may be placed on the outer surface of the catheter to modify at least one physical property of the catheter.

Abstract: A catheter for crossing an occluding lesion with an inflatable balloon and dilating the lesion includes an inner tube that defines a longitudinal axis. The balloon includes a distal section that is bonded to the tube's distal end, a working section, and a conically shaped distal transition section connecting the working and distal section. A plurality of rigid ribs are spaced around the circumference of the balloon near the catheter's distal end. Each rib includes a first elongated portion attached to the balloon's distal section and aligned substantially parallel with the longitudinal axis. A second portion extending from the first portion and at an angle thereto is attached to and lies along the surface of the balloon's distal transition section. The plurality of ribs combine to simulate a stiff, tapered surface that can be wedged into the occluding lesion to create a passageway to cross the lesion with the balloon.

Abstract: An intravascular material delivery dilation catheter having a pair of longitudinally spaced inflatable balloons with a drug delivery region defined therebetween. The catheter is ideally suited for use after a PTCA procedure, wherein the proximate balloon seals the blood vessel while the distal balloon is uniquely contoured when inflated to define fluid communication paths therepast and proximate a blood vessel to be treated. The distal balloon, when inflated, has four lobes but could also be textured. Each lobe is separated from the next by a groove, which groove in combination with the blood vessel inner wall forms a fluid communication path therebetween. Upon inflation of both balloons in a blood vessel, a medicament such as heparin can be injected, via the drug delivery region between the inflated balloons, wherein the medicament flows past the distal balloon at a selected rate.