Abstract: A system used to entrap clots in arteries, such as cerebral arteries, between the artery wall and an external surface of a stent to provide restoration of blood flow therethrough that includes a stent forming an annular wall that defines a set of openings, and an expansion member extendable through the stent to place a distal portion thereof distal to the stent. The stent is advanced into a clot disposed within a vessel and transitioned to an expanded configuration such that the annular wall engages the clot. The expansion member extends through the stent and is transitioned to an expanded state such that a diameter of the distal portion is greater than a diameter of a proximal portion thereof. The expanded distal portion is sized to fill a portion of the vessel to prevent clot fragments from flowing distal to the expansion member.

Abstract: An instrument for deploying an implantable medical device into a body lumen is disclosed. The instrument comprises a base member having a base handle and a deployment extension, a first tubular member having a first tubular body and a first handle, and a second tubular member having a second tubular body and a second handle. The first tubular member fits over the deployment extension and is longitudinally slidable over the deployment extension, and the second tubular member fits over the first tubular member and is longitudinally slidable over the first tubular member. The distal ends of the deployment extension, the first tubular body, and the second tubular body are adapted to hold and deploy the implantable medical device.

Abstract: An instrument for deploying an implantable medical device into a body lumen is disclosed. The instrument comprises a base member having a base handle and a deployment extension, a first tubular member having a first tubular body and a first handle, and a second tubular member having a second tubular body and a second handle. The first tubular member fits over the deployment extension and is longitudinally slidable over the deployment extension, and the second tubular member fits over the first tubular member and is longitudinally slidable over the first tubular member. The distal ends of the deployment extension, the first tubular body, and the second tubular body are adapted to hold and deploy the implantable medical device.

Abstract: A stent in the form of a generally tubular body has multiple annularly expandable serpentine elements. The serpentine elements have arcs at the first and second element ends which point in the axial direction of the stent. Annularly expandable serpentine elements which follow one another in the axial direction are connected to one another via connectors which are arranged at the ends of the adjacent elements. The connectors extend in the circumferential direction of the stent in the non-expanded state of the stent and have a curvature in the circumferential direction. In the expanded state of the stent, the curvature is so great in the circumferential direction that the connectors project radially outward beyond the circumference of the serpentine elements.

Abstract: An instrument for deploying an implantable medical device into a body lumen is disclosed. The instrument comprises a base member having a base handle and a deployment extension, a first tubular member having a first tubular body and a first handle, and a second tubular member having a second tubular body and a second handle. The first tubular member fits over the deployment extension and is longitudinally slidable over the deployment extension, and the second tubular member fits over the first tubular member and is longitudinally slidable over the first tubular member. The distal ends of the deployment extension, the first tubular body, and the second tubular body are adapted to hold and deploy the implantable medical device.

Abstract: An instrument for deploying an implantable medical device into a body lumen is disclosed. The instrument comprises a base member having a base handle and a deployment extension, a first tubular member having a first tubular body and a first handle, and a second tubular member having a second tubular body and a second handle. The first tubular member fits over the deployment extension and is longitudinally slidable over the deployment extension, and the second tubular member fits over the first tubular member and is longitudinally slidable over the first tubular member. The distal ends of the deployment extension, the first tubular body, and the second tubular body are adapted to hold and deploy the implantable medical device.

Abstract: A stent in the form of a generally tubular body has multiple annularly expandable serpentine elements. The serpentine elements have arcs at the first and second element ends which point in the axial direction of the stent. Annularly expandable serpentine elements which follow one another in the axial direction are connected to one another via connectors which are arranged at the ends of the adjacent elements. The connectors extend in the circumferential direction of the stent in the non-expanded state of the stent and have a curvature in the circumferential direction. In the expanded state of the stent, the curvature is so great in the circumferential direction that the connectors project radially outward beyond the circumference of the serpentine elements.

Abstract: A flexible stent and method for performing a stent within a lumen proximate to a target area is provided. The stent includes a tubular member having proximal and distal ends, where at least a portion of the tubular member is capable of being positioned proximate to the target area. The stent also includes a plurality of stabilization members defined circumferentially about at least a portion of the tubular member, wherein each stabilization member extends inwardly to define an inner diameter that is less than an inner diameter of the tubular member within the tubular member. As a result, the stabilization members are capable of reducing migration of the stent within the lumen and the incident of infolding of the tubular member.

Abstract: A stent and associated method for implanting a stent within a body conduit are provided. According to one embodiment, the stent includes a plurality of annular segments arranged peripherally along a longitudinal axis to define opposing free ends, wherein each annular segment includes a plurality of interconnected segment struts. The stent also includes a plurality of connector struts each extending along the longitudinal axis between, and connecting, adjacent annular segments, wherein each connector strut includes an axial section and a compensating section. In addition, at least a portion of each of the segment struts, axial sections, and compensating sections is curved.

Abstract: The invention relates to a radially expandable vessel support (100) comprising a supporting body (102) having a plurality of longitudinally arranged ring segments as well as terminal supporting segments (103) and at least one terminal edge segment (104) arranged at a terminal supporting segment (103), with the terminal supporting segments (103) having a meandering configuration with a multitude of supporting arches (108) and the edge segment or segments (104) having a plurality of relief arches (106), with the number of the relief arches (106) being lower than the number of the supporting arches (108) and the relief arches (106) beginning at the peripheral/edge-situated reversal points (116) of the supporting arches (108).

Abstract: A stent for positioning within a lumen is provided. The stent includes a stent region and a pair of transition regions extending from respective ends of the stent region, wherein each of the transition and stent regions define an aperture therethrough. At least a portion of at least one of the transition regions is configured in a helix including a plurality of turns, wherein the stent region is capable of expanding to conform to a stricture and each of the transition regions is capable of expanding to conform to the lumen proximally and distally of the stricture.

Abstract: A stent for facilitating flow between a branch of a bifurcated lumen and an interior region of the stent is provided. The stent includes proximal and distal ends and an interior region defined therethrough. The stent typically includes scaffolding having a cover applied thereto. The stent also includes at least one drainage region having at least one drainage hole defined between the scaffolding and through the cover such that fluid is capable of flowing through the drainage holes. The drainage region is typically offset from the proximal and/or distal end to facilitate fluid flow between the branch of the bifurcated lumen and the interior region of the stent.

Abstract: The invention is relative to a stent with a tubular support frame consisting of axially successively following, interconnected annular segments, which support frame is surrounded on its outside by a thread. The thread ends are guided via a deflection from the outside into support frame, where they are coupled by a connector consisting of a material visible in x-rays. Deflection is realized by two deflection elements in the form of eyelets provided on annular segment. Deflection elements are arranged on the circumference of support frame at an interval from one another and are provided on end-side annular segment, viewed in longitudinal direction L of the stent.

Abstract: An instrument for deploying an implantable medical device into a body lumen is disclosed. The instrument comprises a base member having a base handle and a deployment extension, a first tubular member having a first tubular body and a first handle, and a second tubular member having a second tubular body and a second handle. The first tubular member fits over the deployment extension and is longitudinally slidable over the deployment extension, and the second tubular member fits over the first tubular member and is longitudinally slidable over the first tubular member. The distal ends of the deployment extension, the first tubular body, and the second tubular body are adapted to hold and deploy the implantable medical device.

Abstract: The invention is relative to a stent with a tubular support frame consisting of axially successively following, interconnected annular segments which support frame is surrounded on its outside by a thread. The thread ends are guided via a deflection from the outside into support frame, where they are coupled by a connector consisting of a material visible in x-rays. Deflection is realized by two deflection elements in the form of eyelets provided on annular segments. Deflection elements are arranged on the circumference of support frame at an interval from one another and are provided on end-side annular segments, viewed in longitudinal direction of the stent.

Abstract: A stent (1) is a vascular prosthesis for a constricted body vessel. The stent (1) includes a tubular support frame (2) of ring segments (3) arranged in axial succession and formed by struts (5, 6) which in initial state are joined continuously in a wave-like manner. Adjacent ring segments (3) are linked by differently long connectors (9, 10) with U-shaped compensating sections (11, 12). All connectors (9, 10) point in the same circumferential direction (U). Moreover, differently long connectors (9, 10) alternate in circumferential direction (U) as well as in longitudinal stent axis (L).

Abstract: Disclosed is a stent (1) representing a prosthesis for a constricted body vessel. The stent (1) includes a tubular support frame (2) composed of ring segments (3, 4, 5) which are sequentially arranged in axial direction and which are formed by segment struts (5, 6) that are continuously joined to one another in the initial state via transitions (8). Adjacent ring segments (3-5) are coupled to each other using tie bars (9, 10). In order to prevent notch stress in the segment struts (5, 6), the width thereof increases from midsection (16) in the direction of the transitions (8), wherein the segment struts (6, 7) are curved in a wave-like manner.

Abstract: Temporary stent having a plurality of ring elements arranged adjacent to each other, with said stent being capable of being explanted after it has been implanted in a body lumen, with all ring elements (3a, b, c, . . . ) starting out from a spine (2) extending over the length of the stent (1) and comprising at least two weakened areas (4, 5, 6) which enable the ring elements (3a, b, c, . . . ) to be collapsible during the process of explantation of the stent, and said spline (2) being provided with a recovery element (8) at its proximal end (7).

Abstract: Embodiments of the present invention relate to a balloon dilatation catheter, in particular for percutaneous transluminal coronary angioplasty (PTCA), provided with a guide wire, a supply tube extending parallel to the guide wire and serving for inflating a dilatation balloon, as well as the dilatation balloon arranged in the distal area of the supply tube, wherein the dilatation balloon has a tubular configuration with a wall structure comprising a plurality of tube segments arranged adjacent to each other of which at least one is connected with the supply tube.

Abstract: Disclosed is a stent (1) representing a prosthesis for a constricted body vessel. The stent (1) includes a tubular support frame (2) composed of ring segments (3, 4, 5) which are sequentially arranged in axial direction and which are formed by segment struts (5, 6) that are continuously joined to one another in the initial state via transitions (8). Adjacent ring segments (3-5) are coupled to each other using tie bars (9, 10). In order to prevent notch stress in the segment struts (5, 6), the width thereof increases from midsection (16) in the direction of the transitions (8), wherein the segment struts (6, 7) are curved in a wave-like manner.