ISO/TC 194
| Reģistrācijas numurs (WIID) | Projekta Nr. | Nosaukums | Statuss |
|---|---|---|---|
| 86799 | ISO/DIS 10993-11 | Biological evaluation of medical devices — Part 11: Tests for systemic toxicity | Aptauja slēgta |
| 86868 | ISO/DIS 21762 | Medical devices utilizing non-viable human materials — Risk management | Aptauja slēgta |
| 71514 | ISO/TS 21726:2019 | Évaluation biologique des dispositifs médicaux — Application du seuil de préoccupation toxicologique (TTC) pour évaluer la biocompatibilité des substances extractibles des dispositifs médicaux | Standarts spēkā |
| 86862 | ISO 10993-4:2017/Amd 1:2025 | Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood — Amendment 1 | Standarts spēkā |
| 84512 | ISO 10993-1:2025 | Biological evaluation of medical devices — Part 1: Requirements and general principles for the evaluation of biological safety within a risk management process | Standarts spēkā |
| 83916 | ISO/TS 11796:2023 | Biological evaluation of medical devices — Requirements for interlaboratory studies to demonstrate the applicability of validated in vitro methods to assess the skin sensitization of medical devices | Standarts spēkā |
| 64582 | ISO 10993-16:2017 | Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachables | Standarts spēkā |
| 44050 | ISO 10993-13:2010 | Évaluation biologique des dispositifs médicaux — Partie 13: Identification et quantification de produits de dégradation de dispositifs médicaux à base de polymères | Standarts spēkā |
| 71690 | ISO 14155:2020 | Investigation clinique des dispositifs médicaux pour sujets humains — Bonne pratique clinique | Standarts spēkā |
| 73582 | ISO/TS 37137-1:2021 | Biological evaluation of absorbable medical devices — Part 1: General requirements | Standarts spēkā |
Attēlo no 121. līdz 130. no pavisam 155 ieraksta(-iem).