A biocompatible medical device is provided having at least one surface, wherein at least a part of said surface is coated with a biocompatible layer configured to provide visibility of said device in X-rays.

A biocompatible medical device is provided having at least one surface, wherein at least a part of said surface is coated with a biocompatible layer configured to provide visibility of said device in X-rays.

A high molecular weight polyethylene polymer is formulated so that the polymer is capable of being injection molded. The polyethylene polymer has a Viscosity Number of greater than about 400 ml/g and has a melt flow rate of greater than about 0.9 g/10 min. The polyethylene polymer is of high purity and is particularly well suited for producing medical products.

Magnetic resonance (MR) visible markers for use in MR-guided placement of brachytherapy seeds, and for use in other MR-guided interventional procedures, are described. The MR-visible markers generally include a tube in which an absorbent thread assembly is disposed. The tube is made fluid-tight by sealing it at both ends with suitable end plugs. The absorbent thread assembly is soaked in a suitable MR-visible fluid.

A coated medical device (10) including a structure (12) adapted for introduction into a passage or vessel of a patient. The structure is formed of preferably a non-porous base material (14) having a bioactive material layer (18) disposed thereon. The medical device is preferably an implantable stent or balloon (26) of which the bioactive material layer is deposited thereon. The stent can be positioned around the balloon and another layer of the bioactive material posited over the entire structure and extending beyond the ends of the positioned stent. The ends of the balloon extend beyond the ends of the stent and include the bioactive material thereon for delivering the bioactive material to the cells of a vessel wall coming in contact therewith. The balloon further includes a layer of hydrophilic material (58) positioned between the base and bioactive material layers of the balloon.

A coated medical device (10) including a structure (12) adapted for introduction into a passage or vessel of a patient. The structure is formed of preferably a non-porous base material (14) having a bioactive material layer (18) disposed thereon. The medical device is preferably an implantable stent or balloon (26) of which the bioactive material layer is deposited thereon. The stent can be positioned around the balloon and another layer of the bioactive material posited over the entire structure and extending beyond the ends of the positioned stent. The ends of the balloon extend beyond the ends of the stent and include the bioactive material thereon for delivering the bioactive material to the cells of a vessel wall coming in contact therewith. The balloon further includes a layer of hydrophilic material (58) positioned between the base and bioactive material layers of the balloon.

High strength biomedical materials and processes for making the same are disclosed. Included in the disclosure are nanoporous hydrophilic solids that can be extruded with a high aspect ratio to make high strength medical catheters and other devices with lubricious and biocompatible surfaces. Biologically active agents may be entrapped in pores of materials to provide a controlled release of the biologically active agent.

An apparatus for treating a cardiac structural and vascular condition. The apparatus includes a catheter and a balloon disposed on the catheter. The balloon further includes a contrast medium covering the outer surface of the balloon, A method for treating a patient. A method for making a balloon with a contrast medium on an outer surface of the balloon.

An apparatus for treating a cardiac structural and vascular condition. The apparatus includes a catheter and a balloon disposed on the catheter. The balloon further includes a contrast medium covering the outer surface of the balloon, A method for treating a patient. A method for making a balloon with a contrast medium on an outer surface of the balloon.

An inner tube includes a tubular body made of a first resin and a reinforcing member disposed on an inner side of the tubular body. The reinforcing member is configured of a linear body including a second resin. The inner tube has a first region including a distal portion provided with a distal opening portion and a second region that is disposed to be closer to a proximal side than the first region. The linear body projects inwardly from the inner surface of the tubular body in the first and second regions, and inwardly projects less in the first region than in the second region. In a balloon catheter, guide wire operability is improved and problems which can arise when using a metal reinforcing member are avoided. In a medical elongated body, sliding resistance of a medical device inserted in a lumen can be reduced.