ISO/TC 194
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 64582 | ISO 10993-16:2017 | Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachables | Standarts spēkā |
| 55614 | ISO 10993-3:2014 | Biological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity | Standarts spēkā |
| 86868 | ISO/DIS 21762 | Medical devices utilizing non-viable human materials — Risk management | Aptauja slēgta |
| 88206 | ISO/DIS 10993-16 | Biological evaluation of medical devices — Part 16: Toxicokinetic evaluation for degradation products and leachables | Aptauja slēgta |
| 85514 | ISO/DIS 18969 | Clinical evaluation of medical devices | Aptauja slēgta |
| 86799 | ISO/DIS 10993-11.2 | Biological evaluation of medical devices — Part 11: Tests for systemic toxicity | Aptauja |
| 32217 | ISO 14155-2:2003 | Clinical investigation of medical devices for human subjects — Part 2: Clinical investigation plans | Atcelts |
| 23955 | ISO 10993-17:2002 | Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substances | Atcelts |
| 31723 | ISO 14155-1:2003 | Clinical investigation of medical devices for human subjects — Part 1: General requirements | Atcelts |
| 18963 | ISO 10993-4:1992 | Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood | Atcelts |
Displaying 31-40 of 157 results.