Abstract: A system for crimping a prosthesis is disclosed, comprising a plurality of wheels. Each wheel has an outer circumferential surface configured to be placed in contact with the prosthesis. When in contact with the prosthesis, each wheel is configured to be rotated, thereby to apply a radially inward force on the prosthesis so as to reduce the diameter of the prosthesis. More than one set of wheels may be provided, so that the prosthesis is crimped first by one set of wheels, then by a subsequent set of wheels.

Abstract: The present invention relates to a catheter comprising an outer tube; an inner tube; and a balloon fixed at its proximal sleeve to the outer tube and at its distal sleeve to the inner tube, wherein the inner tube comprises an elastic segment.

Abstract: Apparatus is provided for sealing a puncture within a vessel or tissue to provide hemostasis, comprising a first disk coupled to either a second disk or a spring, and sealingly engaged to the vessel or tissue surrounding the puncture. At least the first disk is preferably configured to substantially conform to the profile of the vessel or tissue when deployed. In one embodiment, the disks may be released from engagement with the vessel or tissue to reposition the disks after deployment.

Abstract: A body lumen filter includes a plurality of bistable anchors configured to move between a stable pre-deployed state and a stable deployed state. In the stable deployed state the stable pre-deployed diameter the bistable anchors define a pre-deployed anchor diameter and in the stable deployed diameter the bistable anchors define a deployed anchor diameter, the deployed diameter being larger than the pre-deployed diameter. A filtering structure is operatively associated with the bistable anchors.

Abstract: A catheter is configured to prevent kinking of a catheter during handling or mounting of a pressure device. The catheter has a proximal end of its catheter shaft that is provided with a bending section having a flexibility greater than that of the section of the catheter shaft joining the proximal end.

Abstract: The invention discloses a balloon catheter comprising a catheter shaft, at the distal end of which an inflatable balloon is arranged and at the proximal end of which a connecting piece is arranged, comprising a guiding wire which can be passed through a guiding wire lumen of the catheter shaft from the proximal end to the distal end and through the balloon and an inflation or deflation lumen extending from the proximal end of the catheter shaft to the balloon, wherein a portion of the catheter shaft having a selectable length and extending from the proximal end is provided with a metal reinforcing pipe.

Abstract: A method for connecting a catheter balloon with a catheter shaft of a balloon catheter that improves the welding quality of a weld between the catheter balloon and the catheter shaft of the balloon catheter. Preferably, a welding energy absorbing device is arranged, preferably in the form of a coloured tubing, in the area of a fixation site after attaching a pre-fixation and then to irradiate this welding energy absorbing device with the radiation energy to carry out the welding. After the welding the pre-fixation and the welding energy absorbing device are removed.

Abstract: Apparatus and methods for stenting are provided comprising a stent attached to a porous biocompatible material that is permeable to endothelial cell ingrowth, but impermeable to release of emboli of predetermined size. Preferred stent designs are provided, as well as preferred manufacturing techniques. Apparatus and methods are also provided for use at a vessel branching. Moreover, embodiments of the present invention may comprise a coating configured for localized delivery of therapeutic agents. Embodiments of the present invention are expected to provide enhanced embolic protection, improved force distribution, and improved recrossability, while reducing a risk of restenosis and thrombus formation.

Abstract: Methods and devices are provided for the localized administration to a patient of moieties effective for inhibiting unwanted cellular growth, including restenosis of an artery treated with a stent implant for blockage of blood flow by an atherosclerotic lesion. After implantation of a medical device capable of moiety-binding, moieties effective at inhibiting unwanted cellular growth are administered locally to a patient. In this manner the deleterious side-effects of systemic administration of moieties are avoided. Upon localized administration, the moieties bind the medical device, rendering the medical device itself capable of inhibiting unwanted cellular growth. According to an embodiment, after implantation of a stent, radioactive moieties specific for receptors immobilized on the stent surface are locally administered using a balloon perfusion catheter.

Abstract: A catheter balloon is configured to improve its fold-in or collapsing behavior. The catheter balloon has a balloon body portion, a first tapered end portion and a second tapered end portion. The balloon body portion has a substantially cylindrical shape in an expanded state. The first tapered end portion is formed at a first end of the balloon body portion. The first tapered end portion includes a first predetermined embossment. The second tapered end portion is formed at a second end of the balloon body portion. The second tapered end portion includes a second predetermined embossment. The balloon body portion is formed free of a predetermined embossment. In other words, the balloon body portion is formed without folds so that there is only predetermined folding on the conical end portions for inducing the folding of the balloon body portion in a predetermined direction upon collapsing.

Abstract: The present invention relates to a surgical catheter, and more particularly, a balloon catheter having an auxiliary lumen configured to permit the advancement of a functional measurement wire to a treatment site. The auxiliary lumen communicates with a working lumen that is configured to permit the advancement of a guidewire and the functional measurement wire, so that the guidewire and functional measurement wire may selectively be advanced to the treatment site during a surgical procedure.

Abstract: Apparatus and methods for stenting are provided comprising a stent attached to a porous biocompatible material that is permeable to endothelial cell ingrowth, but impermeable to release of emboli of predetermined size. Preferred stent designs are provided, as well as preferred manufacturing techniques. Apparatus and methods are also provided for use at a vessel branching. Moreover, embodiments of the present invention may comprise a coating configured for localized delivery of therapeutic agents. Embodiments of the present invention are expected to provide enhanced embolic protection, improved force distribution, and improved recrossability, while reducing a risk of restenosis and thrombus formation.

Abstract: A catheter basically has a catheter shaft in which a catheter tip of which is provided with a joint made of a material which is more flexible than the material of the catheter shaft. The joint is disposed between the distal end of the catheter shaft and the distal end of the catheter tip. The front end consists of a material being the same or more rigid than that of the catheter shaft.

Abstract: The present invention relates a vascular prosthesis and related assembly methods that includes a plurality of modular segments inter-engaged by flexible, and preferably lockable, inter-engageable elements forming joints or other connector areas. The segments may have a number of different mechanical properties and may be assembled by the clinician, through mechanical or chemical joining, to customize the prosthesis for a specific patient or application.

Abstract: A stent is disclosed that generates an elevated degree of scaffolding to a bodily vessel while retaining a highly flexible structure. In one embodiment, a stent includes an essentially tubular body formed by a web structure that is configured to expand from a contracted delivery configuration to an expanded deployed configuration and that is composed of a plurality of longitudinally adjacent web rings. Those web rings are formed by a plurality of web elements disposed circumferentially around the longitudinal axis of the stent and adjoined one to the other with a junction bend. Each junction bend in a first web ring is coupled to another junction bend in a neighboring ring with as-shaped connector, and the coupled junction bends are not longitudinally aligned but are instead laterally offset.

Abstract: The present invention refers to medical devices comprising a modified Co-Polymer or to the modified Co-Polymer itself having high flexibility and high stress resistance, especially tensile strength or tear resistance, in addition to the good physical characteristics of a Block-Co-Polymers of a polyamide and a polycarbonate diamine.

Abstract: The present invention provides a vascular prosthesis featuring a plurality of modular segments interengaged by flexible, and preferably lockable, inter-engageable elements forming joints. The segments may have a number of different mechanical properties and may be assembled by the clinician to customize the prosthesis for a specific patient or application.

Abstract: The present invention relates to a catheter having a soft distal tip that can be manufactured at lower cost than catheters in the prior art. In one embodiment, the catheter is produced by coupling a soft sleeve to the distal end of a catheter tube. The sleeve may affixed to the catheter tube under temperature and pressure conditions that cause the proximal end of the sleeve to taper against the outer surface of the catheter tube, avoiding or minimizing discontinuities in the insertion profile of the catheter, and that also cause the inner wall of the sleeve to taper against the distal end of the catheter tube, avoiding or minimizing discontinuities in the lumen of the catheter.

Abstract: Apparatus is provided for sealing a vascular puncture by causing a reduction in the circumference of the puncture tract through delivery of a closure agent into tissue surrounding the puncture tract. A resultant inflammatory response and volumetric increase cause the tissue to swell into the puncture tract, thereby sealing it.

Abstract: A catheter basically has a catheter shaft in which a catheter tip of which is provided with a joint made of a material which is more flexible than the material of the catheter shaft. The joint is disposed between the distal end of the catheter shaft and the distal end of the catheter tip. The front end consists of a material being the same or more rigid than that of the catheter shaft.