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Cross References: BS 6254:1989*BS 6255:1989*BS 6256:1989*BS 6257:1997*BS 6871:1989*EN 285*EN 556*prEN 837-1*prEN 868-2*prEN 868-3*prEN 868-4 *prEN 868-5*prEN 868-6*prEN 868-7*prEN 868-8*prEN 1041*prEN 1422*EN 46001*EN 46002*EN ISO 9001*EN ISO 9002*prEN ISO 10993-1 *ISO 5636-2*ISO 5636-5*ISO 9001*ISO 9002 *ISO/DIS 10993-1*ISO 11607*93/42/EEC*ASTM F 1608*DIN 58953-6:1987*SS 876 0019*EN 550*EN 552*EN 554*EN 20187*ISO 187 *
 

Document History

  1. BS EN ISO 11607-1:2020+A11:2022


    Packaging for terminally sterilized medical devices-Requirements for materials, sterile barrier systems and packaging systems

    • Most Recent
  2. BS EN ISO 11607-1:2020


    Packaging for terminally sterilized medical devices-Requirements for materials, sterile barrier systems and packaging systems

    • Historical Version
  3. BS EN ISO 11607-1:2020 Draft


    Draft -- Packaging for terminally sterilized medical devices-Requirements for materials, sterile barrier systems and packaging systems

    • Historical Version
  4. BS EN ISO 11607-1:2017 - TC


    Tracked Changes. Packaging for terminally sterilized medical devices. Requirements for materials, sterile barrier systems and packaging systems

    • Historical Version
  5. BS EN ISO 11607-1:2017


    Packaging for terminally sterilized medical devices-Requirements for materials, sterile barrier systems and packaging systems

    • Historical Version
  6. BS EN ISO 11607-1:2009+A1:2014


    Packaging for terminally sterilized medical devices-Requirements for materials, sterile barrier systems and packaging systems

    • Historical Version
  7. BS EN ISO 11607-1:2009


    Packaging for terminally sterilized medical devices. Requirements for materials, sterile barrier systems and packaging systems

    • Historical Version
  8. BS EN ISO 11607-1:2006


    Packaging for terminally sterilized medical devices-Requirements for materials, sterile barrier systems and packaging systems

    • Historical Version
  9. BS EN 868-1:1997

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    Packaging materials and systems for medical devices which are to be sterilized-General requirements and test methods

    • Historical Version