Abstract: The medical lead delivery device combines features of a guidewire and a stylet in order to more easily and quickly deliver a lead to or through the coronary vein of a patient's heart. The medical lead delivery device includes an elongated body, a controller, a first and second spring, and a sleeve. The elongated body includes a proximal end and a distal end. The controller is disposed at the proximal end and provides enhanced control of the distal tip of the elongated body.

Abstract: The medical lead delivery device more easily and quickly delivers a lead to or through the coronary vein of a patient's heart. The medical lead delivery device includes an elongated body, a controller, a first and second spring, and a sleeve. The elongated body includes a proximal end and a distal end. The controller is disposed at the proximal end and provides enhanced control of the distal tip of the elongated body.

Abstract: The medical lead delivery device combines features of a guidewire and a stylet in order to more easily and quickly deliver a lead to the left ventricle of a patient's heart. The medical lead delivery device includes an elongated body, a controller, a first and second spring, and a sleeve. The elongated body includes a proximal end and a distal end. The controller is disposed at the proximal end and provides enhanced control of the distal tip of the elongated body.

Abstract: The present invention comprises a catheter method of manufacture. The method includes the provision of a subassembly of a lubricious liner and reinforcement. Over the subassembly, a shaft tube, transition tube, and soft tip tube are placed in an abutting relationship to each other, forming an assembly. A first tube of heat shrink is advanced over the assembly, heat is applied to fuse the assembly, and the first heat shrink is removed. Subsequently, the soft tip of the catheter is shaped using a second tube of heat shrink, which is placed over the distal end of the assembly. Heat is applied to the second heat shrink to cause the tip material to flow and to draw the tip material over the distal end of the lubricious liner. The second heat shrink is removed, completing the catheter manufacture.

Abstract: The present invention comprises a catheter and method of manufacture. The catheter includes an elongated core having a unitary lubricous liner and a reinforcement. The lubricous liner defines at least one lumen. The lubricous liner has the reinforcement over the its outer diameter and fused to the lubricous liner. The reinforcement terminates proximal to the distal end of the lubricous liner. The catheter also has an elongated shaft tube which defines a shaft tube lumen. The shaft tube lumen is sized to receive the core, the core which extends longitudinally through the shaft tube lumen. The shaft tube is fused to the core. The catheter also has an elongated transition tube which defines a transition tube lumen. The transition tube lumen is sized to receive the core which extends longitudinally through the transition tube lumen. The distal end of the shaft tube is fused to the proximal end of the transition tube. The transition tube is made of softer material than the shaft tube and is fused to the core.

Abstract: A catheter adapted for placement within a living anatomy, such as the human coronary arterial system, comprises a proximal portion, a first arcuate portion, a second arcuate portion, and a distal tip. The catheter is shaped so that with the distal tip engaged in the coronary ostium, the ellipsoidal shaped second arcuate portion is in contact with the contralateral wall of the aorta, the catheter thus resisting forces tending to displace the distal tip from the ostium.

Abstract: The invention includes an exchange system, a guidewire anchoring means and a method of use for catheters exchangeable over a guidewire (55). The guidewire anchoring means restricts movement between the guidewire (55) and the anchoring means. The anchoring means comprises a shaft (35) with a longitudinal lumen (80) therethrough, the lumen (80) being in fluid communication with a balloon (25 or 30) disposed on the distal end of the shaft (35). A tubular split housing (5 or 10) surrounds the distal end of the shaft (35) and adheres to the balloon (25 or 30), the balloon (25 or 30) being sized to expand to a larger size than the inside diameter of the split housing (5 or 10). The inside diameter of the split housing (5 or 10) is sized to slidably receive a catheter, while the outside diameter of the split housing (5 or 10) is sized to slidably fit within a guide catheter (50 ).