CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 9487 | LVS EN ISO 10993-13:2000 | Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices | Atcelts |
| 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 |
| 9484 | LVS EN ISO 10993-2:2000 | Biological evaluation of medical devices - Part 2: Animal welfare requirements | Atcelts |
| 9482 | LVS EN ISO 10993-9:2000 | Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products | Atcelts |
| 9481 | LVS EN ISO 10993-7:2000 | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals | Atcelts |
| 9477 | LVS EN ISO 10993-10:1995 | Biological evalution of medical devices - Part 10: Tests for irritation and sensitization | Atcelts |
| 9471 | LVS 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 |
| 60214 | EN ISO 22442-2:2015 | Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO/FDIS 22442-2:2015) | Atcelts |
| 79539 | EN ISO 14155:2020/A11:2024 | Clinical investigation of medical devices for human subjects - Good clinical practice | Atcelts |
| 9479 | LVS EN 30993-4:1993 | Biological evalution of medical devices - Part 4: Selection of tests for interactions with blood | Atcelts |
Displaying 81-90 of 195 results.