Abstract: The present invention provides Dental implant configured to be inserted into a hole in jaw bone and to be at least partially situated in bone tissue when implanted, comprising: a coronal implant region, the surface of which is at least partly covered by an oxide layer with an average thickness in the range from 60 nm to 170 nm and has an average arithmetical mean height Sa in the range from 0.1 ?m to 1.0 ?m. Further provided is a component for dental applications, preferably dental abutment, wherein the surface of the component is at least partly covered by an oxide layer with an average thickness in the range from 60 nm to 170 nm and has an average arithmetical mean height Sa in the range from 0.05 ?m to 0.5 ?m and an implant system comprising the dental implant and the component. Method for forming a protective layer on the surface of an implantable or implant component, the method comprising a) applying a solution on the surface of component, the solution having a pH at 25° C. of 6.

Abstract: The present invention provides Dental implant configured to be inserted into a hole in jaw bone and to be at least partially situated in bone tissue when implanted, comprising: a coronal implant region, the surface of which is at least partly covered by an oxide layer with an average thickness in the range from 60 nm to 170 nm and has an average arithmetical mean height Sa in the range from 0.1 ?m to 1.0 ?m. Further provided is a component for dental applications, preferably dental abutment, wherein the surface of the component is at least partly covered by an oxide layer with an average thickness in the range from 60 nm to 170 nm and has an average arithmetical mean height Sa in the range from 0.05 ?m to 0.5 ?m and an implant system comprising the dental implant and the component. Method for forming a protective layer on the surface of an implantable or implant component, the method comprising a) applying a solution on the surface of component, the solution having a pH at 25° C. of 6.

Abstract: The invention relates to a polymer structure (1) formed by at least a polymer, wherein said structure (1) comprises a volume (2) and a surface (3), wherein said polymer comprises a plurality of polymer chains connected by linkings, characterized by a linking density, wherein said linking density increases, particularly monotonously, from the surface (3) into the volume (2) of the polymer structure (1).

Abstract: Disclosed embodiments relate to a membrane closure device (100) for closing a perforation in a membrane (10), comprising: a patch guiding mechanism (110) for guiding at least one expandable patch (120) to a perforation site (12) of a membrane (10); and a fastener delivery mechanism (130, 330) for delivering a fastener (140) to the perforation site (12) and for fastening the at least one expandable patch by the fastener (140) to the membrane (10) to seal the perforation in the membrane (10) by the at least one expandable patch (120).

Abstract: The invention relates to a method, a device and a system for producing particularly a hydrogel (200) and for controlling an enzymatically catalyzed formation of a covalent bond in a solution, wherein said covalent bond is formed between a first compound (20) comprising a first moiety (21) and a second compound (22) comprising a second moiety (23), wherein the first and the second moiety (21, 23) are a substrate of an enzyme wherein said enzyme catalyzes the formation of a covalent bond between the first and the second moiety (21, 23), and wherein a voltage is applied to the solution for spatially controlling said formation, wherein said voltage is adjusted such that it induces electrolysis of said solution.

Abstract: A method and a device that determines surface characteristics of a stent to be implanted in a lumen in a body in which a wetting behavior of a stent surface serves as measure for the surface characteristics of the stent surface. In order to determine the wetting behavior, a course of a wetting force along a length of the stent surface is determined, the wetting power between the stent surface and a liquid surface being detected along the length of the stent.

Abstract: An implant for vascular implantation in a body is provided with a surface which, in the implanted state, is provided for contact with the body or with a bodily fluid and which is at least for the most part hydrated. The surface is advantageously provided as a bare metal surface of a chromium-containing alloy. The vascular implant is used to regulate an adsorption of proteins on the surface of the implant, in respect of the type, quantity and/or conformation of certain proteins, by a defined surface which is at least for the most part hydrated.

Abstract: An implant for implantation into a body is provided with a surface that is provided for contact with the body or a bodily fluid when implanted and which surface has a first surface charge when in a first state. The surface assumes a second state having a second surface charge as a result of surface treatment, the second surface charge being a lower positive surface charge or a higher negative surface charge than the first surface charge. The implant is used for regulating an adsorption of proteins on the surface of the implant in terms of type, quantity and/or conformation of certain proteins by means of a defined second state of the surface, which has a defined second surface charge and/or a defined predetermined composition of an oxide layer of the surface.

Abstract: The invention relates to a polymer structure (1) formed by at least a polymer, wherein said structure (1) comprises a volume (2) and a surface (3), wherein said polymer comprises a plurality of polymer chains connected by linkings, characterized by a linking density, wherein said linking density increases, particularly monotonously, from the surface (3) into the volume (2) of the polymer structure (1).

Abstract: The invention relates to a method, a device and a system for producing particularly a hydrogel (200) and for controlling an enzymatically catalysed formation of a covalent bond in a solution, wherein said covalent bond is formed between a first compound (20) comprising a first moiety (21) and a second compound (22) comprising a second moiety (23), wherein the first and the second moiety (21, 23) are a substrate of an enzyme wherein said enzyme catalyzes the formation of a covalent bond between the first and the second moiety (21, 23), and wherein a voltage is applied to the solution for spatially controlling said formation, wherein said voltage is adjusted such that it induces electrolysis of said solution.

Abstract: A method and an arrangement are disclosed for providing an implant for implantation in a body lumen, that include at least one processing unit (1) for processing the implant (7; 103), a sheathing (2) with a front opening (3) and a rear opening (4), which is at least partially disposed at or in the processing unit (1), and at least one power unit (5). The implant (7; 103) can be stored inside the sheathing (2) between the openings (3, 4). The power unit (5) serves for generation of a current (P) of a defined medium through the sheathing (2), which is connected at least to one opening (3; 4) of the sheathing (2), whereby the current (P) flows inside the sheathing (2) with the stent (7; 103).

Abstract: A method and a device that determines surface characteristics of a stent to be implanted in a lumen in a body in which a wetting behavior of a stent surface serves as measure for the surface characteristics of the stent surface. In order to determine the wetting behavior, a course of a wetting force along a length of the stent surface is determined, the wetting power between the stent surface and a liquid surface being detected along the length of the stent.