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ICS:11.080.01
“ISO 20857:2010 Sterilization of health care products – Dry heat – Requirements for the development, validation and routine control of a sterilization process for medical devices” has been added to your cart. View cart
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ISO 25424:2022 Sterilization of health care products – Low temperature steam and formaldehyde – Requirements for development, validation and routine control of a sterilization process for medical devices – Amendment 1
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ISO 20857:2010 Sterilization of health care products – Dry heat – Requirements for the development, validation and routine control of a sterilization process for medical devices
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ISO 13408:2006 Aseptic processing of health care products – Part 3: Lyophilization
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ISO 11140:2007 Sterilization of health care products – Chemical indicators – Part 5: Class 2 indicators for Bowie and Dick-type air removal tests
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ISO 11140:2014 Sterilization of health care products – Chemical indicators – Part 1: General requirements
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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 18362:2016 Manufacture of cell-based health care products – Control of microbial risks during processing
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ISO 11138:2021 Sterilization of health care products – Biological indicators – Part 8: Method for validation of a reduced incubation time for a biological indicator
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ISO 13408:2018 Aseptic processing of health care products – Part 2: Sterilizing filtration
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