CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 31979 | EN ISO 10993-4:2009 | Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2002, including Amd 1:2006) | Atcelts |
| 31978 | EN ISO 10993-3:2009 | Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2003) | Atcelts |
| 37559 | EN ISO 14155:2011 | Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011) | Atcelts |
| 9482 | EN ISO 10993-9:1999 | Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:1999) | 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 |
| 24852 | EN ISO 10993-12:2007 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2007) | Atcelts |
| 22132 | EN ISO 10993-2:2006 | Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:2006) | Atcelts |
| 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 |
Displaying 91-100 of 194 results.