Registration number (WIID)Project No.TitleStatus
38073LVS EN ISO 20857:2013Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 20857:2010)Standarts spēkā
65050LVS EN ISO 13408-6:2021Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2021)Standarts spēkā
58414EN ISO 13408-2:2018Aseptic processing of health care products - Part 2: Sterilizing filtration (ISO 13408-2:2018)Standarts spēkā
35151LVS EN ISO 13408-3:2011Aseptic processing of health care products - Part 3: Lyophilization (ISO 13408-3:2006)Standarts spēkā
65357EN ISO 14160:2021Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization process for medical devices (ISO 14160:2020)Standarts spēkā
72618EN 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
76997LVS CEN ISO/TS 11137-4:2023Sterilization of health care products - Radiation - Part 4: Guidance on process control (ISO/TS 11137-4:2020)Standarts spēkā
60761EN ISO 11137-1:2015Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006, including Amd 1:2013)Standarts spēkā
72687LVS EN ISO 11137-2:2015/A1:2023Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose - Amendment 1 (ISO 11137-2:2013/Amd 1:2022)Standarts spēkā
68466EN ISO 13408-1:2024Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2023)Standarts spēkā
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