BS EN ISO 11607-2:2020
Withdrawn
Packaging for terminally sterilized medical devices Validation requirements for forming, sealing and assembly processes
Hardcopy , PDF
English
01-20-2020
09-13-2022
| Committee |
CH/198
|
| DocumentType |
Standard
|
| ISBN |
9780539038385
|
| Pages |
24
|
| ProductNote |
THIS STANDARD ALSO REFERS TO :ISO 11607-1:2018
|
| PublisherName |
British Standards Institution
|
| Status |
Withdrawn
|
| Supersedes |
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 assembly of preformed sterile barrier systems, sterile barrier systems and packaging systems.
It is applicable to industry, to health care facilities, and to wherever medical devices are packaged and sterilized.
It does not cover all requirements for packaging medical devices that are manufactured aseptically. Additional requirements can be necessary for drug/device combinations.
| Standards | Relationship |
| EN ISO 11607-2:2020 | Identical |
| ISO 11607-2:2019 | Identical |
| EN ISO 11607-2:2017 | Identical |
| DIN EN ISO 11607-2:2020-05 | Equivalent |
| I.S. EN ISO 11607-2:2020 | Equivalent |
| UNE-EN ISO 11607-2:2020 | Equivalent |
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