ISO/TC 194
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 55614 | ISO 10993-3:2014 | Biological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity | Standarts spēkā |
| 75323 | ISO 10993-17:2023 | Biological evaluation of medical devices — Part 17: Toxicological risk assessment of medical device constituents | Standarts spēkā |
| 68426 | ISO 10993-11:2017 | Biological evaluation of medical devices — Part 11: Tests for systemic toxicity | Standarts spēkā |
| 85514 | ISO/DIS 18969 | Clinical evaluation of medical devices | Aptauja slēgta |
| 88206 | ISO/DIS 10993-16 | Biological evaluation of medical devices — Part 16: Toxicokinetic evaluation for degradation products and leachables | Aptauja slēgta |
| 86868 | ISO/DIS 21762 | Medical devices utilizing non-viable human materials — Risk management | Aptauja slēgta |
| 86799 | ISO/DIS 10993-11 | Biological evaluation of medical devices — Part 11: Tests for systemic toxicity | Aptauja slēgta |
| 45367 | ISO 10993-16:2010 | Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachables | Atcelts |
| 40384 | ISO 10993-12:2007 | Biological evaluation of medical devices — Part 12: Sample preparation and reference materials | Atcelts |
| 22692 | ISO 10993-13:1998 | Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices | Atcelts |
Displaying 31-40 of 156 results.