CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 81042 | prEN ISO 8250 | Cleanliness of medical devices - Process design and test methods | Izstrādē |
| 9485 | - | Biological evaluation of medical devices - Glutaraldehyde and formaldehyde residuals | Izstrādē |
| 77182 | prEN ISO 14155 | Clinical investigation of medical devices for human subjects - Good clinical practice (ISO/DIS 14155:2024) | Izstrādē |
| 77335 | prEN ISO 18969 | Clinical evaluation of medical devices | Izstrādē |
| 9483 | - | Biological evaluation of medical devices - Methods of testing for degradation products | Izstrādē |
| 23327 | LVS EN ISO 10993-4:2003 /A1:2006 | Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood | Atcelts |
| 9499 | LVS EN ISO 10993-17:2003 | Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances | Atcelts |
| 9498 | LVS EN ISO 10993-8:2001 | Biological evaluation of medical devices - Part 8: Selection and qualification of reference materials for biological tests | Atcelts |
| 9496 | LVS EN ISO 10993-4:2003 | Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood | Atcelts |
| 22598 | LVS EN ISO 10993-1:2003 | Biological evaluation of medical devices - Part 1: Evaluation and testing | Atcelts |
Displaying 21-30 of 190 results.