UNE-EN ISO 11607-2:2020
Current
The latest, up-to-date edition.
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2019)
Hardcopy , PDF
23-09-2020
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, and assembly of preformed sterile barrier systems, sterile barrier systems and packaging systems.This part of ISO 11607 is applicable to industry, to health care facilities, and wherever medical devices are packaged and sterilized.This part of ISO 11607 does not cover all requirements for packaging medical devices that are manufactured aseptically. Additional requirements may also be necessary for drug/device combinations.
| Committee |
CTN 111
|
| DocumentType |
Standard
|
| Pages |
22
|
| ProductNote |
THIS STANDARD IS ALSO REFERS TO: ISO 11607-1:2018; ANSI/AAMI ST65; ANSI/AAMI ST77
|
| PublisherName |
Asociación Española de Normalización
|
| Status |
Current
|
| Standards | Relationship |
| EN ISO 11607-2:2020 | Identical |
| ISO 11607-2:2019 | Identical |
| BS 6340-4:1984 | Identical |
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