CEN/TC 204
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 27791 | EN ISO 14937:2009 | 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 |
| 82923 | EN ISO 14937:2009/prA1 | 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 — Amendment 1 | Izstrādē |
| 72618 | 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 |
| 9298 | EN ISO 17664:2004 | Sterilization of medical devices - Information to be provided by the manufacturer for the processing of resterilizable medical devices (ISO 17664:2004) | Atcelts |
| 41915 | EN ISO 17664:2017 | Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices (ISO 17664:2017) | Atcelts |
| 76989 | EN ISO 17664-2:2023 | Processing 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 |
| 9305 | EN ISO 17665-1:2006 | Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665-1:2006) | Atcelts |
| 71095 | EN ISO 17665:2024 | Sterilization of health care products - Moist heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665:2024) | Standarts spēkā |
| 82958 | EN ISO 17665:2024/prA1 | Sterilization of health care products — Moist heat — Requirements for the development, validation and routine control of a sterilization process for medical devices — Amendment 1 | Izstrādē |
| 38073 | EN ISO 20857:2013 | Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 20857:2010) | Standarts spēkā |
Displaying 71-80 of 176 results.