Registration number (WIID)Project No.TitleStatus
35153EN ISO 13408-6:2011Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2005)Atcelts
37341EN ISO 13408-6:2011/A1:2013Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2005/Amd 1:2013)Atcelts
65050EN ISO 13408-6:2021Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2021)Standarts spēkā
40897EN ISO 13408-7:2015Aseptic processing of health care products - Part 7: Alternative processes for medical devices and combination products (ISO 13408-7:2012)Standarts spēkā
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
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
65357EN ISO 14160:2021Sterilization 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 14160:2020)Standarts spēkā
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
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
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
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