ICS:11.080.01

“ISO 11137:2020 Sterilization of health care products – Radiation – Part 4: Guidance on process control” has been added to your cart. View cart

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ISO 11135:2014 Sterilization of health-care products – Ethylene oxide – Requirements for the development, validation and routine control of a sterilization process for medical devices
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ISO 11135:2018 Sterilization of health-care products – Ethylene oxide – Requirements for the development, validation and routine control of a sterilization process for medical devices – Amendment 1: Revision of Annex E, Single batch release
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ISO 11137:2006 Sterilization of health care products – Radiation – Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
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ISO 11137:2013 Sterilization of health care products – Radiation – Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices – Amendment 1
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ISO 11137:2013 Sterilization of health care products – Radiation – Part 2: Establishing the sterilization dose
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ISO 11137:2017 Sterilization of health care products – Radiation – Part 3: Guidance on dosimetric aspects of development, validation and routine control
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ISO 11137:2018 Sterilization of health care products – Radiation – Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices – Amendment 2: Revision to 4.3.4 and 11.2
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ISO 11137:2020 Sterilization of health care products – Radiation – Part 4: Guidance on process control
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ISO 11137:2022 Sterilization of health care products – Radiation – Part 2: Establishing the sterilization dose – Amendment 1
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ISO 11135:2014 Sterilization of health-care products – Ethylene oxide – Requirements for the development, validation and routine control of a sterilization process for medical devices

ISO 11135:2018 Sterilization of health-care products – Ethylene oxide – Requirements for the development, validation and routine control of a sterilization process for medical devices – Amendment 1: Revision of Annex E, Single batch release

ISO 11137:2006 Sterilization of health care products – Radiation – Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices

ISO 11137:2013 Sterilization of health care products – Radiation – Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices – Amendment 1

ISO 11137:2013 Sterilization of health care products – Radiation – Part 2: Establishing the sterilization dose

ISO 11137:2017 Sterilization of health care products – Radiation – Part 3: Guidance on dosimetric aspects of development, validation and routine control

ISO 11137:2018 Sterilization of health care products – Radiation – Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices – Amendment 2: Revision to 4.3.4 and 11.2

ISO 11137:2020 Sterilization of health care products – Radiation – Part 4: Guidance on process control

ISO 11137:2022 Sterilization of health care products – Radiation – Part 2: Establishing the sterilization dose – Amendment 1

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