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Norm

ISO 11607-2:2019

Ausgabedatum: 2019 01 31

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...
Gültig
Herausgeber:
International Organization for Standardization
Format:
Digital | 13 Seiten
Sprache:
Englisch

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.

ISO 11607-2:2019
2019 01 31
Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, s...
Norm
ISO 11607-2:2006/Amd 1:2014
2014 07 07
Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, s...
Norm
ISO 11607-2:2006
2006 04 07
Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, s...
Norm
ISO 11607:2003
2003 02 10
Packaging for terminally sterilized medical devices
Norm
ISO 11607:1997
1997 01 30
Packaging for terminally sterilized medical devices
Norm
Historie aufklappen
Norm
ISO 11607-2:2019/Amd 1:2023
Ausgabedatum : 2023 09 13
Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes — Amendment 1: Application of risk management