CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 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 |
| 9478 | EN ISO 10993-11:1995 | Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:1993) | Atcelts |
| 21140 | EN ISO 10993-12:2004 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2002) | 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 |
| 60721 | EN ISO 10993-1:2020 | Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO/DIS 10993-1:2017) | Atcelts |
| 30062 | EN ISO 10993-16:2010 | Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO/DIS 10993-16:2008) | 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 |
| 32008 | EN ISO 10993-12:2009 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2007) | Atcelts |
| 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 |
| 9497 | EN ISO 10993-5:1999 | Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:1999) | Atcelts |
Displaying 51-60 of 195 results.