Registration number (WIID)Project No.TitleStatus
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
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
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 11135:2023)Izstrādē
72619FprEN ISO 11137-1Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO/DIS 11137-1:2023)Izstrādē
80418prEN ISO 11137-2 revSterilization of health care products — Radiation — Part 2: Establishing the sterilization doseIzstrādē
80410EN ISO 13408-1:2024/prA1Aseptic processing of health care products — Part 1: General requirements — Amendment 1Izstrādē
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
9291-Method(s) of bioburden determination - Methods for validating bioburden techniquesIzstrādē
83953prEN ISO 25224.2Sterilization of health care products — Sampling and culturing for reusable, flexible endoscopesIzstrādē
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