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
26001LVS EN 15424:2007Sterilization of medical devices - Development, validation and routine control of sterilization processes - Low Temperature Steam and FormaldehydeAtcelts
9298LVS EN ISO 17664:2004Sterilization of medical devices - Information to be provided by the manufacturer for the reprocessing of resterilizable devicesAtcelts
9311EN ISO 11137-3:2006Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects (ISO 11137-3:2006)Atcelts
41106CEN ISO/TS 13004:2014Sterilization of health care products - Radiation - Substantiation of selected sterilization dose: Method VDmaxSD (ISO/TS 13004:2013)Atcelts
21434EN 556-2:2003Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devicesAtcelts
9305LVS EN ISO 17665-1:2006Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devicesAtcelts
9305EN ISO 17665-1:2006Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665-1:2006)Atcelts
9293EN 1174-2:1996Sterilization of medical devices - Estimation of the population of micro-organisms on product - Part 2: GuidanceAtcelts
9297LVS EN ISO 14937:2002Sterilization 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 devicesAtcelts
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