Abstract: A balloon dilatation catheter has a relatively strong proximal tube made of a material such as for example metal hypotubing. The distal end of the catheter includes an inflatable medical device or balloon, an inflation lumen and a guidewire lumen. A transition assembly or stiffening member is positioned between the proximal tube and the distal end section, providing for a flexible transition between the two components of diverse stiffness, namely the proximal tube and the flexible distal end portion. A proximal end of the stiffening member may float within a distal end of the proximal tube but the stiffening member distal end is affixed near its distal end to the shaft. The dilatation catheter may have a rapid exchange configuration, and is generally used in conjunction with a guiding catheter. During a procedure when the catheters are within the vascular system, the portion of the dilatation catheter near the transition readily follows curved portions of the inserted guiding catheter.

Abstract: Systems and methods are described for laser bonding polymer catheter components by using laser energy to create localized heat fusion bonds between two or more polymer catheter components.

Abstract: The present invention consists of a main artery stent (the main stent) that is placed in the main artery and a second stent that is placed into the side branch (the side branch stent), the two stents constituting a complete treatment for a stenosed arterial bifurcation. Both stents are preferably drug eluting. The main stent would optimally be one that has a reasonably small area of each cell after the stent is deployed, but also has a large perimeter length for each cell. The stent delivery system for the side branch stent has an attached main guide wire tube that can be advanced over a main guide wire and a central lumen that is advanced over a guide wire placed into the side branch. The structure of the side branch stent delivery system allows the side branch stent to achieve the correct angular orientation and longitudinal position when it is advanced over the two guide wires.

Abstract: A balloon dilatation catheter has a relatively stiff and strong proximal cannula made of a material such as for example metal hypotubing. The distal end of the catheter includes an inflatable medical device or balloon, an inflation lumen and a guidewire lumen. A transition assembly is positioned between the proximal cannula and the distal end section. This transition assembly has a stiffening member within a transition tube, and provides for a flexible transition between the two components of diverse stiffness, namely the proximal cannula and the flexible distal end portion. A proximal end of the stiffening member may float within a distal end of the proximal cannula, but the stiffening member distal end is affixed to the shaft. The dilatation catheter may have a rapid exchange configuration, and is generally used in conjunction with a guiding catheter.

Abstract: A balloon dilatation catheter has a relatively stiff and strong proximal cannula made of a material such as for example metal hypotubing. The distal end of the catheter includes an inflatable medical device or balloon, an inflation lumen and a guidewire lumen. A transition assembly is positioned between the proximal cannula and the distal end section. This transition assembly has a stiffening member within a transition tube, and provides for a flexible transition between the two components of diverse stiffness, namely the proximal cannula and the flexible distal end portion. A proximal end of the stiffening member may float within a distal end of the proximal cannula, but the stiffening member distal end is affixed to the shaft. The dilatation catheter may have a rapid exchange configuration, and is generally used in conjunction with a guiding catheter.

Abstract: The medical devices of the present invention include polymer blends of polyamide and maleated polyethylene. The polyamide component of the blended materials of the present invention may include both homopolymers and copolymers. The other component of the present invention is preferably HDPE, with the addition of maleic anhydride. Accordingly, the materials of the present invention provide a unique combination of physical properties that are advantageous for use in various devices, including medical devices for maneuvering through the circulatory system. The properties of high-strength, capability of bonding to other polyamides, and kink resistance are retained. In addition, several physical properties and benefits are provided by the materials of the present invention, including low friction, functional groups to bond to low friction services, a range of flexibilities, and low gel counts.

Abstract: The medical devices of the present invention include polymer blends of polyamide and maleated polyethylene. The polyamide component of the blended materials of the present invention may include both homopolymers and copolymers. The other component of the present invention is preferably HDPE, with the addition of maleic anhydride. Accordingly, the materials of the present invention provide a unique combination of physical properties that are advantageous for use in various devices, including medical devices for maneuvering through the circulatory system. The properties of high-strength, capability of bonding to other polyamides, and kink resistance are retained. In addition, several physical properties and benefits are provided by the materials of the present invention, including low friction, functional groups to bond to low friction services, a range of flexibilities, and low gel counts.

Abstract: In a torsion control catheter including a tubular body and a flexible tip connected to the tubular body, the improvement comprising a copolymer catheter tip composition comprising a first monomer of polyamide and a second monomer of polyamide having a lower alkyl side chain group attached to a polyamide backbone. The flexible catheter tip may include one or more tip members, at least one of which may be formed of the copolymer composition.

Abstract: A catheter balloon is manufactured and prepared for use by heating a portion of a thermoplastic tube and pressurizing the lumen of the tube to cause the heated tube portion to stretch. Preferably, a central section of the tube portion is heated to a degree greater than the end sections of the tube portions, so that the central section of the tube portion expands to a thinner wall thickness than the end sections of the tube portion. Thus, when this newly formed, integral balloon is expanded within a patient, the central section thereof tends to expand outwardly first, ahead of the end sections. When such a balloon carries a tubular stent within the patient, the early expansion of the central section against a longitudinally centered stent causes a central portion of the stent to expand outwardly first, keeping the stent firmly centered on the balloon as it is expanded by the balloon.

Abstract: A catheter balloon is prepared for inflation, and the balloon is inflated by the following process. At least a portion of an elastic, thermoplastic tube is radially stretched until the radially stretched tube portion exhibits a desired increase in molecular orientation. The stretching conditions, such as selective heating, preferably cause a central section of the stretched tube portion to have less wall thickness than end sections of the tube portion. At least part of the tube portion may be longitudinally stretched relative to the tube, to create a desired biaxial molecular orientation. Thereafter, the tube portion is optionally placed into a stent, the tube portion being part of a catheter. The tube portion is inserted into a patient to position the stent and tube portion at a desired position, such as a location in the coronary artery.

Abstract: A catheter balloon is prepared for inflation, and the balloon is inflated by the following process. At least a portion of an elastic, thermoplastic tube is radially stretched until the radially stretched tube portion exhibits a desired increase in molecular orientation. The stretching conditions, such as selective heating, preferably cause a central section of the stretched tube portion to have less wall thickness than end sections of the tube portion. At least part of the tube portion may be longitudinally stretched relative to the tube, to create a desired biaxial molecular orientation. Thereafter, the tube portion is optionally placed into a stent, the tube portion being part of a catheter. The tube portion is inserted into a patient to position the stent and tube portion at a desired position, such as a location in the coronary artery.