ISO/TC 194
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 68937 | ISO 10993-15:2019 | Biological evaluation of medical devices — Part 15: Identification and quantification of degradation products from metals and alloys | Standarts spēkā |
| 88200 | ISO 10993-23:2021/Amd 1:2025 | Biological evaluation of medical devices — Part 23: Tests for irritation — Amendment 1: Additional in vitro reconstructed human epidermis models | Standarts spēkā |
| 86868 | ISO/DIS 21762 | Medical devices utilizing non-viable human materials — Risk management | Aptauja slēgta |
| 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 |
| 86799 | ISO/DIS 10993-11.2 | Biological evaluation of medical devices — Part 11: Tests for systemic toxicity | Aptauja |
| 68936 | ISO 10993-1:2018 | Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process | Atcelts |
| 21225 | ISO 10993-1:1992/Cor 1:1992 | Biological evaluation of medical devices — Part 1: Guidance on selection of tests — Technical Corrigendum 1 | Atcelts |
| 72766 | ISO 10993-7:2008/Amd 1:2019 | Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals — Amendment 1: Applicability of allowable limits for neonates and infants | Atcelts |
| 31723 | ISO 14155-1:2003 | Clinical investigation of medical devices for human subjects — Part 1: General requirements | Atcelts |
Displaying 31-40 of 157 results.