Registration number (WIID)Project No.TitleStatus
9299EN 13824:2004Sterilization of medical devices - Aseptic processing of liquid medical devices - RequirementsAtcelts
9301EN 556-1:2001Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devicesAtcelts
9311EN ISO 11137-3:2006Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects (ISO 11137-3:2006)Atcelts
9297EN ISO 14937:2000Sterilization 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
9307EN ISO 11737-2:2000Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the validation of a sterilization process (ISO 11737-2:1998)Atcelts
27794EN ISO 14160:2011Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization process for medical devices (ISO/DIS 14160:2009)Atcelts
26001EN 15424:2007Sterilization of medical devices - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devicesAtcelts
35154EN ISO 13408-1:2011Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008)Atcelts
35155EN ISO 13408-2:2011Aseptic processing of health care products - Part 2: Filtration (ISO 13408-2:2003)Atcelts
35153EN ISO 13408-6:2011Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2005)Atcelts
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