Abstract: The present invention describes a method for producing an implant, in particular an intraluminal endoprosthesis, wherein the base material of the body (5) of the implant has biodegradable metallic material, preferably Mg or an Mg alloy. The method comprises the following steps: a. Provide the body (5) of the implant, b. Apply a first layer (10), which contains Ca ions and P ions, to at least a part of the surface of the body (5) and c. Apply a second layer (20), which is at least partially permeable for Ca ions and P ions, such that this at least largely covers the first layer (10). Furthermore, a corresponding implant is described, in which the degradation behavior can be controlled through the production according to the invention.

Abstract: The invention relates to a stent with a structure of a biocorrodible magnesium alloy or tungsten alloy, which comprises a multiplicity of web sections connected to one another, wherein (i) the structure has a support structure of a number of first web sections connected to one another, which are designed to perform a function supporting the vascular wall or preserving the mechanical integrity of the stent after an expansion of the stent for a predetermined period of time and (ii) at least one second web section is present, which a) is directly connected to a selected first web section, b) does not perform a function supporting the vascular wall or preserving the mechanical integrity of the stent after the expansion of the stent for the predetermined period of time, and c) has a smaller average grain size than the first web sections of the support structure from (i).

Abstract: An insertion system (100) for a medical device (10), which is situated in an outer sheath (20) upon insertion, the outer sheath (20) at least regionally encompassing an inner shaft. The outer sheath (20) at least regionally has, at least on its inner side (29) facing toward the medical device (10), a structure (22, 32) which is complementary with an external-peripheral segmented structure (12) of the medical device (10) like a bolt-nut connection.

Abstract: The invention relates to an endovascular implant, which is at least largely biodegradable and whose in vivo degradation can be controlled. To achieve this, the implant comprises a tubular base body, open on its end faces and consisting of at least one biodegradable material, said base body having an in vivo, location-dependent first degradation characteristic D1(x), in addition to a coating that covers the base body completely or in sections and consists of a biodegradable material, said coating having an in vivo, location-dependent second degradation characteristic D2(x).

Abstract: An implant having a base body, comprised either entirely or in part of a biocorrodible metallic material wherein at least the parts of the base body having the biocorrodible metallic material are at least partially covered with a coating of a crosslinked CFx layer with an F/C ratio in the range of 0.5 to 1.5.

Abstract: A stent made of nitinol having improved axial or radial stiffness, the stent having a support structure which comprises peripheral struts around the circumference, wherein the peripheral struts are linked to one another in the axial direction via connection struts. The support structure may assume a first compressed state and a second expanded state. The nitinol is in the support structure in a martensitic microstructure in the compressed state and largely in an austenitic microstructure in the second expanded state. One or more support structure sections, however, are entirely or partially in a martensitic microstructure in the second expanded state.

Abstract: A medical implantable stent comprising a main structure (1) composed of deformable struts (2), which are preferably machined from a tubular blank (3) by laser cutting. A fine structure (4) made of a wire-like or thread-like material attached to the struts (2) of the main structure (1).

Abstract: A stent comprising an essentially tubular open supporting structure (4) of interconnected trusses (9), whereby the supporting structure (4) can be widened radially with deformation of the trusses (9) for application of the stent, and predetermined breaking points (14) in the supporting structure (4) for fragmentation of the stent after application, and the ends (10, 11) of the trusses (9) that are adjacent to the respective predetermined breaking point (14) having a joint design and which are provided in the area of the predetermined breaking point (14), such that the ends (10, 11) of the trusses (9) are held together with articulation under an applied pressure with the predetermined breaking point (14) broken.

Abstract: A stent made of a material having a low strength and having a main body circumscribing a cylindrical shape and radially expandable from a contracted starting position into a dilated support position, comprising a) a plurality of support segments disposed around the circumference and arrayed on one another in the axial direction each segment being formed by a strut meandering in its coarse structure in its contracted starting position and having alternately opposing meandering curves expandable into the support position made of flexible material; b) a plurality of axial connectors connecting between zenith points of at least a part of the meandering curves in the axial-parallel direction of the support segments; and c) at least one means for stabilizing the strut coarse structure in its contracted starting position against radial expansion and being automatically detachable upon a radial expansion of the stent.

Abstract: The invention relates to stents made of a material with an elongation at rupture of 30% or less and with a tubular base body which entirely or in parts comprises structural segments which are interconnected in longitudinal direction of the stents by means of transverse connectors and in which the structural segments comprise a zigzagging or undulating structure of a brace which is wrapped around the longitudinal axis of the stent. Due to the mechanical properties of the materials used, adaptation of the stent design is required. This is achieved in that in a turning region of the zigzagging or undulating structure the brace comprises a straight bending section aligned in circumferential direction.

Abstract: The invention concerns a connecting system for connecting a stent to a radiopaque marker. The intention is to provide a connecting system which allows the stent to be connected to a radiopaque marker without a worsening of the mechanical properties of the stent and which at the lowest possible level of structural complication and expenditure provides a holding force which is adequate for probing with and implantation of the stent. That is achieved in that the connecting system includes at least one gripping connection comprising a gripping element and a clamping element.

Abstract: The invention concerns a stent comprising a longitudinal axis (12) and a peripheral wall (14) which is formed at least over a part of the length of the stent (10) by a lattice-like carrier structure (24) which is open at two ends. The carrier structure includes at least one bar (16) extending helically around the longitudinal axis in such a way as to provide a helical primary shape (26) for the peripherally extending bar with more than one helical turn. Besides the helical primary shape (26) the bar has a zigzag-like or meander-shaped secondary shape (30) with reversal points and associated reversal portions (32), between which extend bar portions (34) of the peripherally extending bar with an extension component in the longitudinal direction of the stent.

Abstract: A stent, in particular a coronary stent, for expansion from a first condition into an expanded second condition in which it holds a vessel in an expanded state, comprising a tubular body whose peripheral surface (1) is formed by a number of support portions (2) which extend in the longitudinal direction of the stent and which comprise bar elements (3) which are connected by way of connecting bars (4), wherein there is provided a number of support portion groups (1.1) with at least a first support portion (2.1) and a second support portion (2.2, 2.3) in adjacent relationship in the peripheral direction of the stent, whose bar elements (3.1, 3.2, 3.3) extend in a meander configuration in the longitudinal direction of the stent, and wherein the first engagement points (4.1, 4.2) of first connecting bars (4) engage the first support portion (2.1) and the second engagement points (4.2, 4.4) of the first connecting bars (4) engage the second support portion (2.2, 2.

Abstract: A stent implantation system comprising a catheter and an expandable vessel support which is releasable fixed in the region of the distal end thereof and which has a carrier structure which encloses a cavity open at its distal ends characterized in that the carrier structure of the vessel supports formed by at least two carrier rings which in their non-expanded condition are jointly fixed to the catheter and are not connected together otherwise.

Abstract: A stent, in particular a coronary stent, for expansion from a first condition into an expanded second condition in which it holds a vessel in an expanded state, comprising a tubular body whose peripheral surface (1) is formed by a number of annular support portions (2, 2.1, 2.2, 2.3) comprising bar elements (3, 3.1, 3.2, 3.3) which are connected in the longitudinal direction of the stent by way of connecting bars (4, 4.1, 4.2), wherein the bar elements (3.1) of at least a first support portion (2.1) and a second support portion (2.2) in adjacent relationship in a first direction (6.1) extend in a meander configuration in the peripheral direction of the stent and the connecting bars (4, 4.1, 4.2) to the second support portion (2.2) engage in the region of the turning points (5, 5.2, 5.3) of the first support portion (2.1), which turning points face in the first direction (6.1), wherein at least two adjacent connecting bars (4.1, 4.2) engage respectively in the region of a turning point (5.

Abstract: The invention concerns a stent comprising a longitudinal axis (12) and a peripheral wall (14) which is formed at least over a part of the length of the stent (10) by a lattice-like carrier structure (24) which is open at two ends. The carrier structure includes at least one bar (16) extending helically around the longitudinal axis in such a way as to provide a helical primary shape (26) for the peripherally extending bar with more than one helical turn. Besides the helical primary shape (26) the bar has a zigzag-like or meander-shaped secondary shape (30) with reversal points and associated reversal portions (32), between which extend bar portions (34) of the peripherally extending bar with an extension component in the longitudinal direction of the stent.

Abstract: The invention concerns a method and a device for crimping a stent onto a balloon of a balloon catheter. The stent is arranged on the balloon so that an outside surface of the balloon and an inside surface of the stent contact each other to form a combination of balloon and stent. The combination is compressed to crimp the stent onto the balloon. The invention is distinguished in that the combination is compressed to varying degrees along the longitudinal axis of the combination.

Abstract: The invention concerns a stent, in particular a coronary stent, comprising a tubular portion, wherein openings are provided in the tubular portion. The invention is distinguished in that the openings provided in the tubular portion of the stent are of a substantially T-shaped configuration.

Abstract: A stent, in particular a coronary stent, has at least one first tubular portion, and at least one second tubular portion. The first and second tubular portions are connected together by at least one first connecting means. The stent is distinguished in that the at least one first connecting means is in the form of a double bar.

Abstract: A stent has a tubular portion which has openings that are of a substantially V-shaped configuration.