CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 32006 | EN ISO 10993-6:2009 | Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007) | Atcelts |
| 23724 | EN ISO 10993-10:2002/A1:2006 | Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity - Amendment 1 (ISO 10993-10:2002/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 |
| 62983 | EN ISO 14155:2020 | Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020) | Atcelts |
| 64034 | EN ISO 10993-7:2008/A1:2022 | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals - Amendment 1: Applicability of allowable limits for neonates and infants (ISO 10993-7:2008/Amd 1:2019) | Atcelts |
| 9495 | LVS EN ISO 10993-3:2003 | Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity | Atcelts |
| 21140 | LVS EN ISO 10993-12:2005 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials | Atcelts |
| 22132 | LVS EN ISO 10993-2:2006 | Biological evaluation of medical devices - Part 2: Animal welfare requirements | Atcelts |
| 32007 | LVS EN ISO 10993-11:2009 | Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006) | Atcelts |
| 21797 | LVS EN ISO 10993-11:2006 | Biological evaluation of medical devices - Part 11: Tests for systemic toxicity | Atcelts |
Displaying 121-130 of 200 results.