Registration number (WIID)Project No.TitleStatus
39251LVS EN 556-2:2016Sterilization of medical devices - Requirements for medical devices to be designated ''STERILE" - Part 2: Requirements for aseptically processed medical devicesAtcelts
24012EN ISO 14937:2000/AC:2005Sterilization 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 (ISO 14937:2000)Atcelts
23112EN ISO 14937:2000/AC:2003Sterilization 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 (ISO 14937:2000)Atcelts
9289LVS EN 556:1994Sterilization of medical devices - Requirements for medical devices to be labelled "Sterile"Atcelts
9302LVS EN 552:1994/A1:1999Sterilization of medical devices - Validation and routine control of sterilization by irradiationAtcelts
9306LVS EN 552:1994/A2:2000Sterilization of medical devices - Validation and routine control of sterilization by irradiationAtcelts
35155LVS EN ISO 13408-2:2011Aseptic processing of health care products - Part 2: Filtration (ISO 13408-2:2003)Atcelts
9296EN ISO 14160:1998Sterilization of single-use medical devices incorporating materials of animal origin - Validation and routine control of sterilization by liquid chemical sterilants (ISO 14160:1998)Atcelts
79283prEN ISO 11737-1Sterilization of health care products - Microbiological methods - Part 1: Determination of a population of microorganisms on products (ISO/DIS 11737-1:2026)Aptauja
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)Aptauja slēgta
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