Registration number (WIID)Project No.TitleStatus
37321EN ISO 13408-1:2011/A1:2013Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008/Amd 1:2013)Atcelts
27305EN ISO 11737-1:2006/AC:2009Sterilization of medical devices - Microbiological methods - Part 1: Determination of a population of microorganisms on products (ISO 11737-1:2006/Cor 1:2007)Atcelts
32632EN ISO 11137-2:2007/AC:2009Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2006/Cor 1:2009)Atcelts
60763EN ISO 13408-1:2015Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008, including Amd 1:2013)Atcelts
27633EN 556-1:2001/AC:2006Sterilization of medical devices - Requirements for medical devices to be designated 'STERILE' - Part 1: Requirements for terminally sterilized medical devicesAtcelts
39251EN 556-2:2015Sterilization of medical devices - Requirements for medical devices to be designated ''STERILE" - Part 2: Requirements for aseptically processed medical devicesAtcelts
32635CEN ISO/TS 11135-2:2008/AC:2009Sterilization of health care products - Ethylene oxide - Part 2: Guidance on the application of ISO 11135-1 (ISO/TS 11135-2:2008/Cor 1:2009)Atcelts
80411prEN ISO 11135Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO/DIS 11135:2025)Aptauja
35151EN ISO 13408-3:2011Aseptic processing of health care products - Part 3: Lyophilization (ISO 13408-3:2006)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
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