CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 9501 | EN ISO 10993-10:2002 | Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity (ISO 10993-10:2002) | Atcelts |
| 9498 | EN ISO 10993-8:2000 | Biological evaluation of medical devices - Part 8: Selection and qualification of reference materials for biological tests (ISO 10993-8:2000) | Atcelts |
| 9487 | EN ISO 10993-13:1998 | Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:1998) | Atcelts |
| 9484 | EN ISO 10993-2:1998 | Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:1992) | Atcelts |
| 9479 | EN 30993-4:1993 | Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:1992) | Atcelts |
| 9478 | EN ISO 10993-11:1995 | Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:1993) | Atcelts |
| 60213 | EN ISO 22442-1:2015 | Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management (ISO/FDIS 22442-1:2015) | Atcelts |
| 40815 | EN ISO 10993-4:2017 | Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO/DIS 10993-4:2015) | Atcelts |
| 24852 | EN ISO 10993-12:2007 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2007) | Atcelts |
| 9475 | EN 30993-3:1993 | Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:1992) | Atcelts |
Displaying 41-50 of 194 results.