Registration number (WIID)Project No.TitleStatus
72112LVS EN ISO 25424:2020/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
78154prCEN ISO/TS 17664-3Processing 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 quantitative cleaning classificationIzstrādē
9284prEN 551Sterilization of medical devices - Method for validation and routine control of ethylene oxide sterilization - GuidanceIzstrādē
9286prEN 553Sterilization of medical devices - Method for validation and routine control of sterilization by irradiation - GuidanceIzstrādē
9288prEN 555Sterilization of medical devices - Method for validation and routine control of steam sterilization - GuidanceIzstrādē
72399prEN ISO 11135Sterilization of health care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO/DIS 11135:2024)Izstrādē
80411prEN ISO 11135 revSterilization of health-care products — Ethylene oxide — Requirements for the development, validation and routine control of a sterilization process for medical devicesIzstrādē
31155prEN ISO 11137-2Sterilization of health care products - Radiation - Part 2: Establishing the sterilization doseIzstrādē
80418prEN ISO 11137-2 revSterilization of health care products — Radiation — Part 2: Establishing the sterilization doseIzstrādē
9310prEN ISO 11137-3Sterilization of medical devices - Microbiological methods - Part 3: Guidance on the evaluation and interpretation of bioburden dataIzstrādē
Displaying 161-170 of 173 results.