Registration number (WIID)Project No.TitleStatus
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/Amd 1:2022)Standarts spēkā
72619FprEN ISO 11137-1Sterilization of health care products - Radiation - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO/FDIS 11137-1:2024)Izstrādē
67200FprEN ISO 18362Manufacture of cell-based health care products - Control of microbial risks during processing (ISO 18362:2016)Izstrādē
27133LVS CEN ISO/TS 11135-2:2008Sterilization of health care products - Ethylene oxide - Part 2: Guidance on the application of ISO 11135-1 (ISO/TS 11135-2:2008)Atcelts
32635LVS CEN 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
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
41106LVS CEN ISO/TS 13004:2014Sterilization of health care products - Radiation - Substantiation of selected sterilization dose: Method VDmaxSD (ISO/TS 13004:2013)Atcelts
27134LVS CEN ISO/TS 17665-2:2009Sterilization of health care products - Moist heat - Part 2: Guidance on the application of ISO 17665-1 (ISO 17665-2:2009)Atcelts
9290LVS EN 1174-1:1996Sterilization of medical devices - Estimation of the population of microorganisms on product - Part 1: RequirementsAtcelts
9293LVS EN 1174-2:1996Sterilization of medical devices - Estimation of the population of microorganisms on product - Part 2: GuidanceAtcelts
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