CRIMPING DEVICE AND METHOD FOR MOUNTING A VASCULAR STENT

• US 20130218139A1
• Filed: 01/29/2013
• Published: 08/22/2013
• Est. Priority Date: 02/16/2012
• Status: Abandoned Application

• Current Assignee: Biotronik AG (Biotronik SE & Company KG)
• Original Assignee: Biotronik AG (Biotronik SE & Company KG)
• Inventors: Fargahi, Amir
• Application Number:
  US13/752,892
• Publication Number:
  US 20130218139A1
• Time in Patent Office: Days
• US Class Current: 606/1
• CPC Class Codes: A61B 17/00 Surgical instruments, devices or methods, e.g. tourniquets A61B18/00 takes precedence; contraceptive devices, pessaries, or applicators therefor A61F6/00; eye surgery A61F9/007; ear surgery A61F11/00
• CPC Class Codes: A61F 2/844 folded prior to deployment
• CPC Class Codes: A61F 2/9522 Means for mounting a stent or stent-graft onto or into a placement instrument
• CPC Class Codes: A61F 2/9525 using a funnel

Abstract

A crimping device for mounting a vascular stent, or a heart valve prosthesis introduced in a vascular stent, on an insertion catheter, comprising a forming tool having a rotationally symmetrical forming cavity, which at one end comprises a stent receiving section, at the opposing end a stent outfeed section and in between these a tapering section, and a pushing tool, which comprises a retaining and handling section and a stent forming section, wherein the latter is designed to penetrate the forming cavity of the forming tool from the open end of the stent receiving section and to seize and push back the vascular stent introduced there through the tapering section.

Claims

1. A crimping device for mounting a vascular stent, or a heart valve prosthesis introduced in the vascular stent, on an insertion catheter, comprising:

a forming tool having a rotationally symmetrical forming cavity, which at one end comprises a stent receiving section, at the opposing end a stent outfeed section and in between the stent receiving section and the stent outfeed section, a tapering section, and

a pushing tool, which comprises a retaining and handling section and a stent forming section, wherein the stent forming section is designed to penetrate the forming cavity of the forming tool from an open end of the stent receiving section and to seize and push back the vascular stent introduced in the forming tool through the tapering section.

2. The crimping device according to claim 1, wherein the stent forming section of the pushing tool comprises a plurality of flexible rods, or ribs that are tapered toward free ends of the plurality of flexible rods or ribs, and the retaining and handling section comprises a circular ring-shaped or disk-shaped holder, on a circumference of which the rods or ribs are held on one side, in particular at identical angular distances.

3. The crimping device according to claim 1, wherein the forming tool has a two-piece design that can be folded open.

4. The crimping device according to claim 1, wherein the stent outfeed section is also designed as an outer tube receiving section that receives and fixes an outer tube of the insertion catheter.

5. The crimping device according to claim 4, wherein the outer tube receiving section of the forming tool has a larger diameter than an adjoining end of the tapering section such that an end of the outer tube receiving section forms an annular stop for a distal end of the outer tube of the insertion catheter.

6. The crimping device according to claim 1, wherein the tapering section of the forming tool has a truncated cone shape.

7. The crimping tool according to claim 1, wherein the tapering section of the forming tool is composed of at least two truncated cone-shaped sections having differing cone angles.

8. The crimping device according to claim 1, wherein the wall of the tapering section of the forming tool is curved.

9. The crimping device according to claim 1, wherein the forming tool has at least one section made of transparent material.

10. The crimping device according to claim 1, wherein the forming tool further comprises contact surfaces with a hydrophobic or hydrophilic coating.

11. A method for mounting a vascular stent, or a heart valve prosthesis introduced in the vascular stent, on an insertion catheter, comprising:

providing an expanded vascular stent or a heart valve prosthesis comprising an expanded vascular stent;

providing an insertion catheter comprising an inner tube having a catheter tip and an outer tube that is displaced with respect to the inner tube;

providing a forming tool having a rotationally symmetrical forming cavity, which at one end comprises a stent receiving section, at an opposing end comprises an outer tube receiving section and in between the stent receiving section and the outer tube receiving section, a tapering section;

providing a pushing tool, which comprises a retaining and handling section and a stent forming section, wherein the stent forming section is designed to penetrate the forming cavity of the forming tool from an open end of the stent receiving section and to seize and push back the vascular stent introduced in the forming tool through the tapering section;

introducing the vascular stent or the heart valve prosthesis in the stent receiving section of the forming tool;

introducing a distal end of the insertion catheter in the forming tool, wherein a distal end of the outer tube, in a retracted state, is fixed in the outer tube receiving section of the forming tool; and

inserting the stent forming section of the pushing tool into an open end of the stent receiving section of the forming tool and pushing back the vascular stent or the heart valve prosthesis through the forming cavity while reducing a diameter of the vascular stent or the heart valve prosthesis, and while simultaneously pushing the vascular stent or the heart valve prosthesis between the outer tube and inner tube of the insertion catheter.

12. A crimping device for mounting an implant on an insertion catheter, the device comprising:

a first half shell with a first side;

a second half shell that cooperates with the first half shell, the second half shell having a first side;

at least one hinge arranged about the first half shell first side and the second half shell first side to thereby pivotably connect the first and second half shells wherein they pivotably move about the at least one hinge and have a closed position wherein they abut one another; and

,

a forming cavity defined between the first half shell and the second half shell when they are in the closed position, the forming cavity defining an outer tube receiving section at an open first end, a funnel shaped tapered section adjacent to the tube receiving section, an annular shoulder separating the outer tube receiving section from the adjacent funnel shaped tapered section, and a stent receiving section adjacent to the at least one tapered section and open at a second cavity end.

13. The crimping device according to claim 12 and further comprising:

a pushing tool having a retaining and handling section and a stent forming section, wherein the retaining and handling section is formed as a circular ring or disk, and the stent forming section is formed by a plurality of flexible rods that are attached on one side to the retaining and handling section at identical angular distances, the plurality of flexible rods configured for insertion through the stent receiving section; and

,

wherein the forming cavity is configured to receive the pushing tool inserted into the stent receiving section and pushed toward the tube receiving section.

14. The device according to claim 13, wherein the plurality of flexible rods are tapered toward a free end of the rods, and wherein the forming tool permits visual control of a mounting or crimping process without interim opening of the forming tool.

15. A crimping device according to claim 12 wherein:

the funnel shaped tapered section comprises first and second truncated cone sections, the first truncated cone section having a first diameter that is smaller than the diameter of the tube receiving section to thereby define the annular shoulder between the tube receiving section and the tapered section, the first truncated cone section having an increasing diameter moving along its axial direction away from the tube receiving section;

the second truncated cone section adjacent to the first truncated cone section and having a diameter that is larger than the largest diameter of the first truncated cone section, the second truncated cone section having a gradually increasing diameter moving along its axis in a direction away from the first truncated cone section; and

,

wherein the stent receiving section has a cylindrical shape with a constant diameter that is equal to the largest diameter of the second truncated cone section.

16. A crimping device according to claim 15 wherein the second truncated cone section has a different rate of varying diameter along its axis as compared to the first truncated cone section.

17. The device according to claim 12, wherein the device is configured to receive an insertion catheter having an inner tube, a tip, and an outer tube that are axially displaced with respect to each other, wherein the insertion catheter is placed in the forming tool such that one end of the outer tube is received in the outer tube receiving section.

18. The device according to claim 12, wherein the forming cavity is configured to reduce a diameter of the stent as it is pushed through the forming cavity to a final dimension intended for an implantation process.

19. The device according to claim 12, wherein:

the tapering section comprises a first truncated cone section and a second truncated cone section, the first truncated cone section having a first diameter that is greater than a diameter of the second truncated cone section, the first and second truncated cone sections arranged in sequence to define an increasing diameter moving in an axial direction from the tube receiving section towards the stent receiving section, and, the outer tube receiving section having a diameter that is greater than a diameter of the adjacent second truncated cone section to thereby define the annular shoulder that is configured to receive an outer tube of an insertion catheter.