ISO - 11607-2 AMD 1
Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes AMENDMENT 1: Application of risk management
active, Most Current
| Organization: | ISO |
| Publication Date: | 1 September 2023 |
| Status: | active |
| Page Count: | 12 |
| ICS Code (Sterilized packaging): | 11.080.30 |
Document History
11607-2 AMD 1
September 1, 2023
Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes AMENDMENT 1: Application of risk management
A description is not available for this item.
February 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...
July 15, 2014
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes AMENDMENT 1
A description is not available for this item.
April 15, 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,...