CEN/TC 204
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
72112 | LVS EN ISO 25424:2020/A1:2022 | Sterilization of health care products - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices - Amendment 1 (ISO 25424:2018/Amd 1:2022) | Standarts spēkā |
78154 | prCEN ISO/TS 17664-3 | Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 3: Guidance on the designation of a reusable medical device to a quantitative cleaning classification | Izstrādē |
9284 | prEN 551 | Sterilization of medical devices - Method for validation and routine control of ethylene oxide sterilization - Guidance | Izstrādē |
9286 | prEN 553 | Sterilization of medical devices - Method for validation and routine control of sterilization by irradiation - Guidance | Izstrādē |
9288 | prEN 555 | Sterilization of medical devices - Method for validation and routine control of steam sterilization - Guidance | Izstrādē |
72399 | prEN ISO 11135 | Sterilization of health care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO/DIS 11135:2024) | Izstrādē |
80411 | prEN ISO 11135 rev | Sterilization of health-care products — Ethylene oxide — Requirements for the development, validation and routine control of a sterilization process for medical devices | Izstrādē |
31155 | prEN ISO 11137-2 | Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose | Izstrādē |
80418 | prEN ISO 11137-2 rev | Sterilization of health care products — Radiation — Part 2: Establishing the sterilization dose | Izstrādē |
9310 | prEN ISO 11137-3 | Sterilization of medical devices - Microbiological methods - Part 3: Guidance on the evaluation and interpretation of bioburden data | Izstrādē |
Displaying 161-170 of 173 results.