CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 9489 | EN ISO 10993-15:2000 | Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000) | Atcelts |
| 9500 | EN ISO 10993-18:2005 | Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005) | Atcelts |
| 32001 | EN ISO 10993-15:2009 | Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000) | Atcelts |
| 9471 | EN 30993-1:1994 | Biological evaluation of medical devices - Part 1: Guidance on selection of tests (ISO 10993-1:1992 + Technical Corrigendum 1:1992) | Atcelts |
| 9501 | LVS EN ISO 10993-10:2003 | Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity | Atcelts |
| 9499 | LVS EN ISO 10993-17:2003 | Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances | Atcelts |
| 78812 | prEN ISO 21762 | Medical devices utilizing human tissues and their derivatives -- Application of risk management | Izstrādē |
| 75885 | prEN ISO 10993-7 | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO/DIS 10993-7:2024) | Izstrādē |
| 80889 | prEN ISO 10993-14 rev | Biological evaluation of medical devices — Part 14: Identification and quantification of degradation products from ceramics | Izstrādē |
| 78991 | prEN ISO 10993-16 rev | Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables | Izstrādē |
Displaying 161-170 of 190 results.