Registration number (WIID)Project No.TitleStatus
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
41915EN ISO 17664:2017Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices (ISO 17664:2017)Atcelts
27134LVS CEN ISO/TS 17665-2:2009Sterilization of health care products - Moist heat - Part 2: Guidance on the application of ISO 17665-1 (ISO 17665-2:2009)Atcelts
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
9308EN ISO 11137-1:2006Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006)Atcelts
9298LVS EN ISO 17664:2004Sterilization of medical devices - Information to be provided by the manufacturer for the reprocessing of resterilizable devicesAtcelts
9285EN 552:1994Sterilization of medical devices - Validation and routine control of sterilization by irradiationAtcelts
9300EN 556:1994 + A1:1998Sterilization of medical devices - Requirements for terminally-sterilized medical devices to be labelled "Sterile"Atcelts
9293LVS EN 1174-2:1996Sterilization of medical devices - Estimation of the population of microorganisms 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
Displaying 61-70 of 176 results.