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About This Item
Full Description
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.
Document History
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BS EN ISO 11607-2:2020+A1:2023
Packaging for terminally sterilized medical devices-Validation requirements for forming, sealing and assembly processes- Most Recent
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BS EN ISO 11607-2:2020+A11:2022
Packaging for terminally sterilized medical devices-Validation requirements for forming, sealing and assembly processes- Historical Version
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BS EN ISO 11607-2:2020
viewing
Packaging for terminally sterilized medical devices-Validation requirements for forming, sealing and assembly processes- Historical Version
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BS EN ISO 11607-2:2017
Packaging for terminally sterilized medical devices-Validation requirements for forming, sealing and assembly processes- Historical Version
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BS EN ISO 11607-2:2006+A1:2014
Packaging for terminally sterilized medical devices-Validation requirements for forming, sealing and assembly processes- Historical Version
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BS EN ISO 11607-2:2006
Packaging for terminally sterilized medical devices. Validation requirements for forming, sealing and assembly processes- Historical Version