AENOR - UNE-EN ISO 11607-2/A11
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2019)
active, Most Current
| Organization: | AENOR |
| Publication Date: | 21 December 2022 |
| Status: | active |
| Page Count: | 13 |
| ICS Code (Sterilized packaging): | 11.080.30 |
Document History
UNE-EN ISO 11607-2/A11
December 21, 2022
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2019)
A description is not available for this item.
September 23, 2020
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2019)
A description is not available for this item.
October 11, 2017
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2006, including Amd 1:2014)
A description is not available for this item.
December 23, 2014
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2006/Amd 1:2014)
A description is not available for this item.
March 28, 2007
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2006)
A description is not available for this item.