Protective packaging assembly for medical devices and method of using same

• US 20050252805A1
• Filed: 05/11/2004
• Published: 11/17/2005
• Est. Priority Date: 05/11/2004
• Status: Active Grant

• Current Assignee: Medtronic Vascular, Inc. (Medtronic Plc)
• Original Assignee: Medtronic Vascular, Inc. (Medtronic Plc)
• Inventors: Cervantes, Marvin J.
• Granted Patent: US 7,353,946 B2
• Time in Patent Office: Days
• US Class Current: 206/384
• CPC Class Codes: A61F 2/0095 Packages or dispensers for prostheses or other implants for intraocular lenses A61F2/1691; for dental surgery A61C19/02
• CPC Class Codes: A61F 2/86 Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure
• CPC Class Codes: A61F 2250/0071 breakable or frangible
• CPC Class Codes: A61M 25/002 Packages specially adapted therefor combined with means for introducing catheters, e.g. dispensers, A61M25/0113; catheter kit packages for surgical articles A61B50/30

Abstract

A protective packaging system for a medical device includes a housing and an end cap. The housing surrounds the distal portion of a catheter bearing a medical device so that the device is suspended in a protective chamber. The end cap holds the housing closed. Another embodiment of the invention provides a method for removing a catheter and medical device from the packaging system.

Claims

1. A system for packaging a treatment device comprising:

a housing to receive a distal portion of a catheter carrying a treatment device and to suspend the device in a protective chamber, the housing including a first portion rotatably attached to a second portion to allow rotation between an open and closed position, and

a flexible end cap including an opening formed therein and an interior surface to mate with an end portion of the first and second housing portions in the closed position, the end cap including opposing protrusions extending from a cap surface adjacent a distal end of the end cap, wherein when the protrusions are pressed, a shape of the opening is reconfigured to allow removal of the end cap from the end of the housing.

2. The system of claim 1 wherein the end portion of the housing includes a narrow portion and a tail portion extending radially outward from the narrow portion, the inner surface of the end cap having a configuration complementary to narrow portion and the tail portion.

3. The system of claim 1 further comprising a controlled environment port.

4. The system of claim 1 further comprising at least one sealing member that forms a gas impermeable seal between the catheter and the housing.

5. The system of claim 4 wherein the sealing member maintains an inert gas within the interior of the housing.

6. The system of claim 4 wherein the sealing member maintains a reduced pressure within the interior of the housing.

7. The system of claim 1 wherein the housing comprises a polymeric material selected from a group consisting of polyurethane, polyethylene, high-density polyethylene, nylon, polytetrafluroethylene and combinations thereof.

8. The system of claim 1 wherein the treatment device is a stent.

9. The system of claim 8 wherein the stent is disposed upon an expandable balloon member.

10. The system of claim 8 wherein the stent is a self-expanding stent.

11. The system of claim 8 further comprising a coating on at least a portion of the stent.

12. The system of claim 11 further comprising at least one therapeutic agent dispersed within the coating.

13. The system of claim 11 further comprising at least one biologic agent dispersed within the coating.

14. The system of claim 11 further comprising at least one radiotherapeutic agent dispersed within the coating.

15. The system of claim 11 wherein the housing prevents damage to the coated portion of the stent during handling.

16. The system of claim 1 further comprising a gas permeable liner disposed about the inner surface of the housing.

17. The delivery system of claim 16 wherein the gas permeable liner comprises high-density polyethylene fibers.

18. The delivery system of claim 17 wherein the stent is sterilized using a sterilant selected from the group consisting of ethylene oxide, gamma radiation, electron-beam radiation, steam and chemicals.

19. A method for removing a treatment device from a packaging system, the method comprising:

providing a closed housing enclosing a distal portion of a catheter carrying a treatment device, and an end cap mated to the tail portion of the housing;

flexing an end cap and thereby altering a shape of an end cap opening;

removing the end cap from the housing while the shape of the opening is altered;

opening first and second portions of the housing to allow removal of the distal portion of the catheter carrying the treatment device.

20. The method of claim 19 wherein flexing the tail portion comprises pressing opposing protrusions of the end cap.

21. The method of claim 19 wherein altering the shape of the end cap opening allows the removal of the end cap from the end of the housing.

22. The method of claim 19 wherein opening the first and second portions of the housing comprises rotating a first portion of the housing in relation to a second portion of the housing to an open configuration.