Registration number (WIID)Project No.TitleStatus
71095LVS EN ISO 17665:2024Sterilization of health care products - Moist heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665:2024)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
35748LVS EN ISO 25424:2011Sterilization of medical devices - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 25424:2009)Atcelts
62264LVS EN ISO 25424:2020Sterilization of health care products - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 25424:2018)Standarts spēkā
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
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 11135:2023)Izstrādē
80411prEN 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 11135:2025)Izstrādē
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