CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 22598 | LVS EN ISO 10993-1:2003 | Biological evaluation of medical devices - Part 1: Evaluation and testing | 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 |
| 9500 | LVS EN ISO 10993-18:2005 | Biological evaluation of medical devices - Part 18: Chemical characterization of materials | 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 |
| 21801 | LVS EN ISO 10993-6:2007 | Biological evaluation of medical devices - Part 6: Tests for local effects after implantation | Atcelts |
| 24852 | LVS EN ISO 10993-12:2008 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials | Atcelts |
| 32003 | LVS EN ISO 10993-17:2009 | Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002) | Atcelts |
| 78812 | prEN ISO 21762 | Medical devices utilizing non-viable human materials - Risk management (ISO/DIS 21762:2025) | Aptauja slēgta |
Displaying 121-130 of 195 results.