Abstract: A release device for releasing a medical implant from an insertion device, in which the implant can be released by a relative movement between a first and a second insertion element, wherein the insertion device has a proximal end, which faces the user during use, and a distal end, which is distanced from the user during use. Between the proximal and the distal end, a shortening region is provided, in which, when generating a targeted relative movement between the first and the second insertion element of the insertion device, a length of at least one of the insertion elements between the proximal end and the distal end can be shortened.

Abstract: Packaging has an outer sleeve, which surrounds an interior space for receiving an object, such as a sterilized medical implant. A separate container is arranged in the interior space and surrounds an absorber in a gas-tight manner, such that a gas present in the interior space cannot pass to the absorber. The container is configured to be opened by the application of force when the outer sleeve is closed, such that a gas disposed in the interior space can pass to the absorber and can be absorbed thereby. In preferred embodiments, the absorber absorbs air with the reactive constituents O2 and/or H2O. Depending on the application, however, other gases can also be absorbed by the absorber. A method for packaging is also provided.

Abstract: A bioabsorbable osteosynthesis implant, having a polymeric main body and at least one macroscopic reinforcement structure, which is integrated in the main body and is made of a biodegradable metal or a metal alloy.

Abstract: An implant having a preferably hollow cylindrical basic structure. A nonwoven fabric is disposed in and/or on the basic structure, the nonwoven fabric preferably comprising biocompatible thermoplastic polyurethane and/or a polymer selected from the group consisting of polylactic acid; polycaprolactone, and a copolymer thereof, and/or a polymer including polyphosphazene. At least in at least one section of the implant, preferably at the proximal and/or distal ends of the implant, fastening means are provided or the nonwoven fabric is treated such that, at least in the expanded state of the implant, the protrusion of nonwoven fabric sections from the implant is significantly reduced. Furthermore, a method for producing such an implant is provided.

Abstract: The present invention relates to an implant, in particular an intraluminal endoprothesis, comprising a body containing a metallic material, and comprising at least one functional element that is fastened to the body and has a material composition in at least a portion of its volume that differs from the material of the body, the material composition preferably including radio-opaque and/or x-ray opaque material. To effectively prevent accelerated degradation due to the formation of a local cell of the material of the body and the functional element, the at least one functional element includes a first layer at least in the region of its surface where it is bonded to the body, the first layer primarily containing at least one metal oxide. Furthermore, the manufacture of an implant of this type is described.

Abstract: A system and a method for crimping a heart valve prosthesis onto a catheter shaft. The system comprises two components (1, 2) which receive the heart valve prosthesis (12) and are inserted into one another in the direction (14) in order to crimp the heart valve prosthesis (12).

Abstract: A prosthesis delivery handle with a bushing (66) with two adjacent internal threads (64, 74) with different diameters and pitch surrounding a tubular threaded first shaft member (36) cooperating with the first thread (64) and a second inner member with a protrusion (82) extending through an axial slot in the tubular first member such that the protrusion runs in the second thread (74). First and second members are connected to an external shaft (112) and an internal element (102) so that when the bushing is rotated first and second members travel axially with different speeds the internal shaft and an external shaft move accordingly.

Abstract: An orthopedic implant, such as a bone screw with a self-tapping thread, is formed of a biodegradable material such as a magnesium alloy. A bioactive surface coating is provided on the implant, such as at the threading. The coating contains micro-abrasives which assist with screw/implant penetration, and/or contains microcapsules containing lubricant, wherein the microcapsules rupture from pressure and frictional heat as the implant penetrates bone.

Abstract: The present invention relates to an implant (10), and particularly to an intraluminal endoprosthesis, comprising a body and at least one abluminal layer (3) disposed on the body, the abluminal layer preferably containing at least one pharmaceutically active substance. In order to protect the abluminal layer (3) from delamination or shearing, the abluminal layer (3) is additionally fastened to the implant body at least in a transition region (7) by way of at least one anchoring layer (5) disposed on the abluminal layer (3). In addition, methods for producing such an implant are described.

Abstract: Stent, as well as a method and device for fabricating the stent, wherein the stent has a tubular lattice structure comprising individual struts and at least one strut of which at least one longitudinal section runs with at least one directional component in the radial circumferential direction of the stent, wherein the surface of the longitudinal section facing the outside of the stent is curved only about the longitudinal axis of the stent. According to the invention, the surface of longitudinal section of the strut, which surface faces the inside of the stent, has such a curvature that the strut cross section is fluidically optimized.

Abstract: One embodiment of the invention relates to an implant comprising a base body made of a biocorrodible magnesium alloy. The magnesium alloy contains a plurality of statistically distributed particles, comprising one or more of the elements Y, Zr, Mn, Sc, Fe, Ni, Co, W, Pt and noble earths with the atomic numbers 57 to 71, or the particles comprise alloys or compounds containing one or more of the elements mentioned. The mean distance of the particles from each other is smaller than the hundredfold mean particle diameter.

Abstract: A vascular implant made in total or in parts of a biodegradable magnesium alloy consisting of Y: 2.0-6.0% by weight, Nd: 1.5-4.5% by weight, Gd: 0-4.0% by weight, Dy: 0-4.0% by weight, Er: 0-4.0% by weight, Zr: 0.1-1.0% by weight, Li: 0-0.2% by weight, Al: 0-0.3% by weight, under the condition that a) a total content of Er, Gd and Dy is in the range of 0.82-4.0% by weight and b) a total content of Nd, Er, Gd and Dy is in the range of 2.98-8.5% by weight, the balance being magnesium and incidental impurities up to a total of 0.3% by weight.

Abstract: A bone screw formed primarily of a magnesium alloy has a self-tapping thread, and is prestressed with a retained torsional stress oriented oppositely to the direction in which the screw is screwed into bone. The pre-stressing opposes the torsional stresses arising from screwing in the screw, thereby raising the effective strength of the screw and/or allowing for a reduction in its size/mass.

Abstract: A release device (150, 150a, 150b) for detaching a medical implant (105) from an insertion device (110), comprising a body (10, 10a, 10b) having a proximal end (12), which during use lies furthest from a distal end (120) of the insertion device (110), and a distal end (14), which during use faces the distal end (120) of the insertion device (110), wherein at least one first actuator (16, 18) is provided between the proximal and distal ends (12, 14), wherein the at least first actuator (16, 18) can be tilted about an axis substantially perpendicularly to at least one of the insertion elements (132, 134) so as to effect a targeted relative movement in the longitudinal direction between the first and second insertion elements (132, 134) of the insertion device (110).

Abstract: A crimping tool and method for reducing an external dimension of a compressible prosthetic device, the crimping tool comprising a first member comprising a first control surface collapsible between a first state and a second state, the first member having a first open end configured for introducing the prosthetic device when the first control surface is in the first state, and a second open end configured for allowing locking of the prosthetic device when introduced into the first member; an engagement portion that moves the first control surface from the first state to the second state; and an actuator portion for moving the first member along the longitudinal axis allowing the engagement portion to interact with the first member.

Abstract: A method for producing an implant and the implant itself, particularly an intraluminal endoprosthesis, wherein the implant is produced from a preferably hollow cylindrical semifinished article (10), wherein the semifinished article contains magnesium or a magnesium alloy, the method comprising preparing the semifinished article (10), and shaping the semifinished article at a temperature of between 250° C. and 550° C. using a tool, which has a metallic lubricant containing gallium and/or a gallium compound on at least a part of its surface that will come into contact with the semifinished article.

Abstract: A new class of rapamycin 40-O-cyclic hydrocarbon esters is disclosed. The 40-O position of the rapamycin ester has the form 40-O—R, where R is C(O)—(CH2)n-X, n is 0, 1 or 2, and X is a cyclic hydrocarbon having 3-8 carbons, optionally containing one or more unsaturated bonds, and one or more linear (CH2)) and/or cyclic (X) carbon atoms may have an OH or halide group. Also disclosed are therapeutic compositions and methods that employ the novel analogs.

Abstract: A method for manufacturing an implant and an implant, in particular an intraluminal endoprosthesis, including a body having a coating on at least a portion of the surface thereof, and the degradation of which can be influenced from the outside in a targeted manner, the method having the following steps: a) providing an implant body, and b) applying a coating to the surface of the implant body, wherein the coating comprises unfilled cavities, preferably in the form of microbubbles (2).

Abstract: Catheter devices provide for rolling movement between the inner and outer catheter tubes with a roller assembly in a radial gap between the inner and outer catheter tubes. Devices of the invention are particularly useful in minimally invasive implantations, such as the implantation of a vascular implant. A particular application is interventional catheter-assisted aortic valve implantation.

Abstract: Bioprosthetic components based on, or comprising, biological materials for implants, preferably biological heart valves, in particular biological heart valve leaflets, which have only been chemically or thermally stabilized (partly crosslinked) at mechanically stressed points and therefore have zones having different mechanical properties, and to a method for the production thereof.