Registration number (WIID)Project No.TitleStatus
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
35152LVS EN ISO 13408-5:2011Aseptic processing of health care products - Part 5: Sterilization in place (ISO 13408-5:2006)Standarts spēkā
72687EN 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
35151LVS EN ISO 13408-3:2011Aseptic processing of health care products - Part 3: Lyophilization (ISO 13408-3:2006)Standarts spēkā
68466LVS EN ISO 13408-1:2024Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2023)Standarts spēkā
78154CEN ISO/TS 17664-3:2026Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 3: Guidance on the designation of a reusable medical device to a cleaning classification (ISO/TS 17664-3:2026)Standarts spēkā
27791LVS EN ISO 14937:2010Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices (ISO 14937:2009)Standarts spēkā
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
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
Displaying 141-150 of 180 results.