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 |
| 31982 | EN ISO 10993-10:2009 | Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity (ISO 10993-10:2002, including Amd 1:2006) | Atcelts |
| 32007 | EN ISO 10993-11:2009 | Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006) | Atcelts |
| 32766 | EN ISO 10993-12:2012 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO/DIS 10993-12:2010) | Atcelts |
| 37559 | EN ISO 14155:2011 | Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011) | Atcelts |
| 23327 | EN ISO 10993-4:2002/A1:2006 | Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood - Amendment 1 (ISO 10993-4:2002/Amd 1:2006) | Atcelts |
| 27050 | EN ISO 10993-9:2009 | Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO/FDIS 10993-9:2009) | Atcelts |
| 21140 | EN ISO 10993-12:2004 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2002) | Atcelts |
| 32004 | EN ISO 10993-18:2009 | Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005) | Atcelts |
Displaying 71-80 of 194 results.