AENOR UNE-EN ISO 11607-2
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2006, including Amd 1:2014)
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| Organization: | AENOR |
| Publication Date: | 11 October 2017 |
| Status: | active |
| Page Count: | 27 |
| ICS Code (Sterilized packaging): | 11.080.30 |
Document History
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.
AENOR UNE-EN ISO 11607-2
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.