AAMI - 11607-2
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes
inactive
| Organization: | AAMI |
| Publication Date: | 1 January 2006 |
| Status: | inactive |
| Page Count: | 26 |
Document History
January 1, 2019
Packaging for terminally sterilized medical devices – Part 2: Validation requirements for forming, sealing, and assembly processes
This document specifies requirements for the development and validation of processes for packaging medical devices that are terminally sterilized. These processes include forming, sealing and...
January 1, 2006
Packaging for terminally sterilized medical devices—Part 2: Validation requirements for forming, sealing, and assembly processes
This part of ISO 11607 specifies the requirements for development and validation of processes for packaging medical devices that are terminally sterilized. These processes include forming, sealing,...
January 1, 2006
Packaging for terminally sterilized medical devices-Part 2: Validation requirements for forming, sealing, and assembly processes
This part of ISO 11607 specifies the requirements for development and validation of processes for packaging medical devices that are terminally sterilized. These processes include forming, sealing,...
11607-2
January 1, 2006
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes
A description is not available for this item.