CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 9494 | EN ISO 10993-16:1997 | Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:1997) | Atcelts |
| 32002 | EN ISO 10993-16:2009 | Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:1997) | Atcelts |
| 35184 | EN ISO 10993-1:2009/AC:2010 | Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process - Technical Corrigendum 1 (ISO 10993-1:2009/Cor 1:2010) | Atcelts |
| 32006 | LVS EN ISO 10993-6:2009 | Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007) | Atcelts |
| 31981 | LVS EN ISO 10993-9:2009 | Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:1999) | Atcelts |
| 23327 | LVS EN ISO 10993-4:2003 /A1:2006 | Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood | Atcelts |
| 9497 | LVS EN ISO 10993-5:1999 | Biological evalution of medical devices - Part 5: Tests for in vitro cytotoxicity | Atcelts |
| 31981 | EN ISO 10993-9:2009 | Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:1999) | Atcelts |
| 9478 | LVS EN ISO 10993-11:1995 | Biological evalution of medical devices - Part 11: Tests for systemic toxicity | Atcelts |
| 9486 | LVS EN ISO 10993-12:1996 | Biological evalution of medical devices - Part 12: Sample preparation and reference materials | Atcelts |
Displaying 111-120 of 194 results.