Registration number (WIID)Project No.TitleStatus
68466EN ISO 13408-1:2024Aseptic processing of health care products - Part 1: General requirements (ISO/DIS 13408-1:2021)Standarts spēkā
60761LVS EN 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
35152LVS EN ISO 13408-5:2011Aseptic processing of health care products - Part 5: Sterilization in place (ISO 13408-5:2006)Standarts spēkā
35151LVS EN ISO 13408-3:2011Aseptic processing of health care products - Part 3: Lyophilization (ISO 13408-3:2006)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
62251LVS EN ISO 11737-2:2020Sterilization of health care products - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (ISO 11737-2:2019)Standarts spēkā
72112EN ISO 25424:2019/A1:2022Sterilization 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 (ISO 25424:2018/DAM 1:2021)Standarts spēkā
62262EN ISO 11135:2014/A1:2019Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices - Amendment 1: Revision of Annex E, Single batch release (ISO 11135:2014/DAM 1:2017)Standarts spēkā
58413EN ISO 11737-1:2018Sterilization of health care products - Microbiological methods - Part 1: Determination of a population of microorganisms on product (ISO/DIS 11737-1:2016)Standarts spēkā
62264LVS EN ISO 25424:2020Sterilization 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
Displaying 141-150 of 176 results.