CEN/TC 206
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
31980 | prEN ISO 10993-5 | Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:1999) | Izstrādē |
81042 | prEN ISO 8250 | Cleanliness of medical devices - Process design and test methods | Izstrādē |
40661 | prEN ISO 10993-7 rev | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals | Izstrādē |
31037 | prEN ISO 10993-4 rev | Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO/NP 10993-4:2008) | Izstrādē |
77391 | prEN ISO 10993-6 | Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO/DIS 10993-6:2024) | Izstrādē |
77335 | prEN ISO 18969 | Clinical evaluation of medical devices | Izstrādē |
75596 | prEN ISO 10993-1 | Biological evaluation of medical devices - Part 1: Requirements and general principles for the evaluation of biological safety within a risk management process (ISO/DIS 10993-1:2024) | Izstrādē |
75885 | prEN ISO 10993-7 | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO/DIS 10993-7:2024) | Izstrādē |
9483 | - | Biological evaluation of medical devices - Methods of testing for degradation products | Izstrādē |
73021 | prEN ISO 10993-3 rev | Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive and developmental toxicity | Izstrādē |
Displaying 181-190 of 190 results.