Registration number (WIID)Project No.TitleStatus
9303EN ISO 11135-1:2007Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11135-1:2007)Atcelts
76162EN 556-2:2024Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devicesStandarts spēkā
39251EN 556-2:2015Sterilization of medical devices - Requirements for medical devices to be designated ''STERILE" - Part 2: Requirements for aseptically processed medical devicesAtcelts
21434EN 556-2:2003Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devicesAtcelts
9300EN 556:1994 + A1:1998Sterilization of medical devices - Requirements for terminally-sterilized medical devices to be labelled "Sterile"Atcelts
9289EN 556:1994Sterilization of medical devices - Requirements for medical devices to be labelled "Sterile"Atcelts
76163EN 556-1:2024Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devicesStandarts spēkā
27633EN 556-1:2001/AC:2006Sterilization of medical devices - Requirements for medical devices to be designated 'STERILE' - Part 1: Requirements for terminally sterilized medical devicesAtcelts
9301EN 556-1:2001Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devicesAtcelts
9287EN 554:1994Sterilization of medical devices - Validation and routine control of sterilization by moist heatAtcelts
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