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Cross References:
ISO 10012
ISO 10993-7
ISO 11138-1:2006
ISO 11138-2:2009
ISO 11140-1
ISO 11737-1
ISO 11737-2
ISO 13485:2003/Cor 1:2009
ISO 9000:2005
ISO 9001
ISO 10993
ISO 11607-1
ISO 11607-2
ISO 14001
ISO 14040
ISO 14161:2009
ISO 14937:2009
ISO 14971
ISO 15883
ISO 17664
ISO 22442-1
ISO 22442-2
ISO 22442-3
ISO/IEC Guide 99:2007
ISO/IEC 90003
ISO/TS 11139:2006
ISO/TS 16775
IEC 61010-1
IEC 61010-2-040
ANSI/AAMI ST41:1999
ANSI/AAMI ST67:2006
AAMI TIR15:2009
AAMI TIR16:2009
AAMI TIR28:2009
AS/NZS 4187
EN 556-1
Directive ATEX 94/9/EC
90/385/EEC
93/42/EEC


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

Document History

  1. BS EN ISO 11135:2014+A1:2019


    Sterilization of health-care products. Ethylene oxide. Requirements for the development, validation and routine control of a sterilization process for medical devices

    • Most Recent
  2. BS EN ISO 11135:2014

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    Sterilization of health-care products. Ethylene oxide. Requirements for the development, validation and routine control of a sterilization process for medical devices

    • Historical Version
  3. BS DD CEN ISO/TS 11135-2:2008


    Sterilization of health care products. Ethylene oxide

    • Historical Version
  4. BS 11/30244091 DC


    BS EN ISO 11135. Sterilization of health-care products. Ethylene oxide. Requirements for the development, validation and routine control of a sterilization process for medical devices

    • Historical Version
  5. BS EN ISO 11135-1:2007


    Sterilization of health care products. Ethylene oxide

    • Historical Version
  6. BS EN 550:1994


    Sterilization of medical devices. Validation and routine control of ethylene oxide sterilization

    • Historical Version