Registration number (WIID)Project No.TitleStatus
62264EN ISO 25424:2019Sterilization of health care products - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices (ISO/DIS 25424:2017)Standarts spēkā
76163EN 556-1:2024Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devicesStandarts spēkā
36593LVS EN ISO 11135:2014Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014)Standarts spēkā
68466EN ISO 13408-1:2024Aseptic processing of health care products - Part 1: General requirements (ISO/DIS 13408-1:2021)Standarts spēkā
60762EN ISO 11137-2:2015Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2013)Standarts spēkā
40897EN ISO 13408-7:2015Aseptic processing of health care products - Part 7: Alternative processes for medical devices and combination products (ISO 13408-7:2012)Standarts spēkā
62251EN ISO 11737-2:2020Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (ISO/DIS 11737-2:2018)Standarts spēkā
35152EN ISO 13408-5:2011Aseptic processing of health care products - Part 5: Sterilization in place (ISO 13408-5:2006)Standarts spēkā
72618LVS EN ISO 17664-1:2021Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 1: Critical and semi-critical medical devices (ISO 17664-1:2021)Standarts spēkā
68466LVS EN ISO 13408-1:2024Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2023)Standarts spēkā
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