CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 60725 | LVS EN ISO 10993-18:2020 | Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020) | Standarts spēkā |
| 78991 | prEN ISO 10993-16 | Biological evaluation of medical devices - Part 16: Toxicokinetic evaluation for degradation products and leachables (ISO/DIS 10993-16:2025) | Aptauja slēgta |
| 78812 | prEN ISO 21762 | Medical devices utilizing non-viable human materials - Risk management (ISO/DIS 21762:2025) | Aptauja slēgta |
| 77335 | prEN ISO 18969 | Clinical evaluation of medical devices (ISO/DIS 18969:2025) | Aptauja slēgta |
| 77933 | prEN ISO 10993-11 | Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO/DIS 10993-11:2026) | Aptauja |
| 9501 | LVS EN ISO 10993-10:2003 | Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity | Atcelts |
| 9471 | EN 30993-1:1994 | Biological evaluation of medical devices - Part 1: Guidance on selection of tests (ISO 10993-1:1992 + Technical Corrigendum 1:1992) | Atcelts |
| 32001 | EN ISO 10993-15:2009 | Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000) | Atcelts |
| 9500 | EN ISO 10993-18:2005 | Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005) | Atcelts |
| 9489 | EN ISO 10993-15:2000 | Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000) | Atcelts |
Displaying 61-70 of 198 results.