Registration number (WIID)Project No.TitleStatus
31155prEN ISO 11137-2Sterilization of health care products - Radiation - Part 2: Establishing the sterilization doseIzstrādē
78154FprCEN 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 cleaning classification (ISO/DTS 17664-3:2026)Izstrādē
76997CEN ISO/TS 11137-4:2023Sterilization of health care products - Radiation - Part 4: Guidance on process control (ISO/TS 11137-4:2020)Izstrādē
78646prEN ISO 14937Sterilization 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 devicesIzstrādē
9284prEN 551Sterilization of medical devices - Method for validation and routine control of ethylene oxide sterilization - GuidanceIzstrādē
9310prEN ISO 11137-3Sterilization of medical devices - Microbiological methods - Part 3: Guidance on the evaluation and interpretation of bioburden dataIzstrādē
9288prEN 555Sterilization of medical devices - Method for validation and routine control of steam sterilization - GuidanceIzstrādē
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
82958EN ISO 17665:2024/prA1Sterilization of health care products — Moist heat — Requirements for the development, validation and routine control of a sterilization process for medical devices — Amendment 1Izstrādē
82923EN ISO 14937:2009/prA1Sterilization 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 — Amendment 1Izstrādē
Displaying 1-10 of 179 results.