CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 81042 | prEN ISO 8250 | Cleanliness of medical devices - Process design and test methods | Izstrādē |
| 79217 | EN ISO 10993-7:2008/prA11 | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals | Izstrādē |
| 78988 | prEN ISO 10993-3 | Biological evaluation of medical devices - Part 3: Evaluation of genotoxicity, carcinogenicity, reproductive toxicity, and developmental toxicity (ISO/DIS 10993-3:2025) | Izstrādē |
| 9487 | EN ISO 10993-13:1998 | Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:1998) | Atcelts |
| 9498 | EN ISO 10993-8:2000 | Biological evaluation of medical devices - Part 8: Selection and qualification of reference materials for biological tests (ISO 10993-8:2000) | Atcelts |
| 40624 | EN ISO 10993-10:2013 | Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010) | Atcelts |
| 21801 | EN ISO 10993-6:2007 | Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007) | Atcelts |
| 9475 | EN 30993-3:1993 | Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:1992) | Atcelts |
| 60214 | EN ISO 22442-2:2015 | Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO 22442-2:2015) | Atcelts |
| 60213 | EN ISO 22442-1:2015 | Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management (ISO 22442-1:2015) | Atcelts |
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