connecting system for connecting a stent to a radiopaque marker and a process for the production of a connection between a stent and two or more radiopaque markers

• US 20060241741A1
• Filed: 06/01/2004
• Published: 10/26/2006
• Est. Priority Date: 06/02/2003
• Status: Abandoned Application

• Current Assignee: Biotronik SE & Company KG
• Original Assignee: Biotronik SE & Company KG
• Inventors: Lootz, Daniel
• Application Number:
  US10/559,592
• Publication Number:
  US 20060241741A1
• Time in Patent Office: Days
• US Class Current: 623/1.340
• CPC Class Codes: A61F 2/91 made from perforated sheet material or tubes, e.g. perforated by laser cuts or etched holes
• CPC Class Codes: A61F 2/915 with bands having a meander structure, adjacent bands being connected to each other
• CPC Class Codes: A61F 2002/91533 characterised by the phase between adjacent bands
• CPC Class Codes: A61F 2002/91558 connected peak to peak
• CPC Class Codes: A61F 2230/0054 V-shaped
• CPC Class Codes: A61F 2250/0098 radio-opaque, e.g. radio-opaque markers

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.

Claims

1. A connecting system for connecting a stent to a radiopaque marker, the connecting system comprising at least one gripping connection comprising a gripping element and a clamping element.

2. A connecting system as set forth in claim 1, wherein the radiopaque marker is in the form of a gripping or clamping element of the gripping connection.

3. A connecting system as set forth in claim 1, wherein the marker is formed from a biocompatible material.

4. A connecting system as set forth in claim 3, wherein the marker at least in part comprises one or more metals selected from the group consisting of Ta, Nb, Zr, Hf, Mo, W, Au, Pt, Ir, rare earths and alloys thereof.

5. A connecting system as set forth in claim 4, wherein the marker at least in part comprises PtIr.

6. A connecting system as set forth in claim 1, wherein the gripping or clamping element of the gripping connection is formed on a basic structure of the stent.

7. A connecting system as set forth in claim 6, wherein the connecting system is integrated into the basic structure in such a way that it does not project or projects at most to a slight extent in a radial direction beyond the dimensions of a peripheral wall of the basic structure.

8. A connecting system as set forth in claim 6, wherein the gripping or clamping element is arranged at the proximal end of the stent.

9. A connecting system as set forth in claim 6, wherein the gripping or clamping element is formed from a biodegradable material.

10. A connecting system as set forth in claim 1, wherein the stent is self-expanding.

11. A connecting system as set forth in claim 1, wherein the stent is biodegradable.

12. A connecting system as set forth in claim 11, wherein the stent is formed entirely or in parts from a biodegradable Mg-alloy.

13. A process for the production of a connection between a stent and two or more radiopaque markers by means of a connecting system as set forth in claim 1, wherein:

(a) two or more markers are connected together by way of a positioning element so that the markers are aligned with their gripping or clamping elements with the corresponding gripping or clamping elements of the stent,

(b) in a working step the markers are placed with their gripping or clamping elements on to the corresponding gripping or clamping elements of the stent, and

(c) then the connection between the positioning element and the gripping or clamping elements of the marker is separated.

14. A process for the production of a connection between a stent and two or more radiopaque markers by means of a connecting system as set forth in claim 4, wherein:

(a) two or more markers are connected together by way of a positioning element so that the markers are aligned with their gripping or clamping elements with the corresponding gripping or clamping elements of the stent,

(b) in a working step the markers are placed with their gripping or clamping elements on to the corresponding gripping or clamping elements of the stent, and

(c) then the connection between the positioning element and the gripping or clamping elements of the marker is separated.

15. A process for the production of a connection between a stent and two or more radiopaque markers by means of a connecting system as set forth in claim 9, wherein:

(a) two or more markers are connected together by way of a positioning element so that the markers are aligned with their gripping or clamping elements with the corresponding gripping or clamping elements of the stent,

(b) in a working step the markers are placed with their gripping or clamping elements on to the corresponding gripping or clamping elements of the stent, and

(c) then the connection between the positioning element and the gripping or clamping elements of the marker is separated.

16. A process for the production of a connection between a stent and two or more radiopaque markers by means of a connecting system as set forth in claim 10, wherein:

(a) two or more markers are connected together by way of a positioning element so that the markers are aligned with their gripping or clamping elements with the corresponding gripping or clamping elements of the stent,

(b) in a working step the markers are placed with their gripping or clamping elements on to the corresponding gripping or clamping elements of the stent, and

(c) then the connection between the positioning element and the gripping or clamping elements of the marker is separated.

17. A connecting system as set forth in claim 2, wherein the marker is formed from a biocompatible material.

18. A connecting system as set forth in claim 17, wherein the marker at least in part comprises PtIr.

19. A connecting system as set forth in claim 9, wherein the stent is self-expanding.

20. A connecting system as set forth in claim 19, wherein the stent is biodegradable.