Registration number (WIID)Project No.TitleStatus
68124LVS EN ISO 11737-1:2018/A1:2021Sterilization of health care products - Microbiological methods - Part 1: Determination of a population of microorganisms on products - Amendment 1 (ISO 11737-1:2018/Amd 1:2021)Standarts spēkā
67200FprEN ISO 18362Manufacture of cell-based health care products - Control of microbial risks during processing (ISO 18362:2016)Izstrādē
65418LVS EN ISO 11137-1:2015/A2:2020Sterilization 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 11137-1:2006/Amd 2:2018)Standarts spēkā
65418EN ISO 11137-1:2015/A2:2019Sterilization 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 11137-1:2006/Amd 2:2018)Standarts spēkā
65357LVS EN 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
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
65050EN ISO 13408-6:2021Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2021)Standarts spēkā
65050LVS EN ISO 13408-6:2021Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2021)Standarts spēkā
62287prEN ISO 17665-1 revSterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devicesIzstrādē
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 25424:2018)Standarts spēkā
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