CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 32004 | LVS EN ISO 10993-18:2009 | Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005) | Atcelts |
| 9494 | LVS EN ISO 10993-16:1997 | Biological evalution of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables | Atcelts |
| 9488 | LVS EN ISO 10993-14:2003 | Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics | Atcelts |
| 32766 | LVS EN ISO 10993-12:2012 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012) | Atcelts |
| 9480 | LVS EN 30993-6:1994 | Biological evalution of medical devices - Part 6: Tests for local effects after implantation | Atcelts |
| 35184 | LVS EN ISO 10993-1:2010 /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 |
| 27050 | LVS EN ISO 10993-9:2010 | Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:2009) | Atcelts |
| 9479 | LVS EN 30993-4:1993 | Biological evalution of medical devices - Part 4: Selection of tests for interactions with blood | Atcelts |
| 22132 | LVS EN ISO 10993-2:2006 | Biological evaluation of medical devices - Part 2: Animal welfare requirements | Atcelts |
| 79539 | EN ISO 14155:2020/A11:2024 | Clinical investigation of medical devices for human subjects - Good clinical practice | Atcelts |
Displaying 171-180 of 200 results.
