Registration number (WIID)Project No.TitleStatus
76989EN ISO 17664-2:2023Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 2: Non-critical medical devices (ISO 17664-2:2021)Standarts spēkā
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
9298EN ISO 17664:2004Sterilization of medical devices - Information to be provided by the manufacturer for the processing of resterilizable medical devices (ISO 17664:2004)Atcelts
72618EN ISO 17664-1:2021Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 1: Critical and semi-critical medical devices (ISO 17664-1:2021)Standarts spēkā
82923EN ISO 14937:2009/prA1Sterilization 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 — Amendment 1Izstrādē
27791EN ISO 14937:2009Sterilization 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 14937:2009)Standarts spēkā
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
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
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
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
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