CEN/TC 204
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
9298 | LVS EN ISO 17664:2004 | Sterilization of medical devices - Information to be provided by the manufacturer for the reprocessing of resterilizable devices | Atcelts |
72618 | LVS EN ISO 17664-1:2021 | Processing 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 |
27791 | LVS EN ISO 14937:2010 | Sterilization 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 |
24012 | LVS EN ISO 14937:2002 /AC:2005 | Sterilization 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 | Atcelts |
23112 | LVS EN ISO 14937:2002 /AC:2004 | Sterilization 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 | Atcelts |
9297 | LVS EN ISO 14937:2002 | Sterilization 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 | Atcelts |
65357 | LVS EN ISO 14160:2021 | Sterilization 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 |
27794 | LVS EN ISO 14160:2011 | Sterilization 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 14160:2011) | Atcelts |
9296 | LVS EN ISO 14160:1998 | Sterilization of single-use medical devices incorporating materials of animal origin - Validation and routine control of sterilization by liquid chemical sterilants | Atcelts |
40897 | LVS EN ISO 13408-7:2015 | Aseptic processing of health care products - Part 7: Alternative processes for medical devices and combination products (ISO 13408-7:2012) | Standarts spēkā |
Displaying 21-30 of 173 results.