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About This Item

 

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Cross References:
ISO 11607-1
DIN 58953-8:2003 (G)
ISO 13485:2003 Ed 2
DIN 58953-7:2003 (G)
ISO/TS 11139:2006 Ed 2
DIN 58953-9:2000 (G)
EN 868-8:1999
ISO 9001:2000
ISO 2859-1:1999
EN 868-6:1999
ISO 186:2002
EN 868-5:1999
ISO 9000:2000
EN 13795-1:2002


All current amendments available at time of purchase are included with the purchase of this document.
 

Document History

  1. BS EN ISO 11607-2:2020+A1:2023


    Packaging for terminally sterilized medical devices-Validation requirements for forming, sealing and assembly processes

    • Most Recent
  2. BS EN ISO 11607-2:2020+A11:2022


    Packaging for terminally sterilized medical devices-Validation requirements for forming, sealing and assembly processes

    • Historical Version
  3. BS EN ISO 11607-2:2020


    Packaging for terminally sterilized medical devices-Validation requirements for forming, sealing and assembly processes

    • Historical Version
  4. BS EN ISO 11607-2:2017

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    Packaging for terminally sterilized medical devices-Validation requirements for forming, sealing and assembly processes

    • Historical Version
  5. BS EN ISO 11607-2:2006+A1:2014


    Packaging for terminally sterilized medical devices-Validation requirements for forming, sealing and assembly processes

    • Historical Version
  6. BS EN ISO 11607-2:2006


    Packaging for terminally sterilized medical devices. Validation requirements for forming, sealing and assembly processes

    • Historical Version