Registration number (WIID)Project No.TitleStatus
35154LVS EN ISO 13408-1:2011Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008)Atcelts
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
9307LVS EN ISO 11737-2:2001Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the validation of a sterilization processAtcelts
26001LVS EN 15424:2007Sterilization of medical devices - Development, validation and routine control of sterilization processes - Low Temperature Steam and FormaldehydeAtcelts
9306LVS EN 552:1994/A2:2000Sterilization of medical devices - Validation and routine control of sterilization by irradiationAtcelts
24012LVS EN ISO 14937:2002 /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 devicesAtcelts
21434LVS EN 556-2:2004Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devicesAtcelts
9290LVS EN 1174-1:1996Sterilization of medical devices - Estimation of the population of microorganisms on product - Part 1: RequirementsAtcelts
9301LVS EN 556-1:2002Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devicesAtcelts
9296LVS EN ISO 14160:1998Sterilization of single-use medical devices incorporating materials of animal origin - Validation and routine control of sterilization by liquid chemical sterilantsAtcelts
Displaying 41-50 of 176 results.