CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 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 |
| 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 |
| 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 |
| 9495 | EN ISO 10993-3:2003 | Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2003) | Atcelts |
| 9492 | EN ISO 10993-1:1997 | Biological evaluation of medical devices - Part 1: Evaluation and testing (ISO 10993-1:1997) | Atcelts |
Displaying 131-140 of 195 results.