ISO/TC 194
| Reģistrācijas numurs (WIID) | Projekta Nr. | Nosaukums | Statuss |
|---|---|---|---|
| 61089 | ISO 10993-6:2016 | Évaluation biologique des dispositifs médicaux — Partie 6: Essais concernant les effets locaux après implantation | 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 |
| 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 |
| 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 |
| 55614 | ISO 10993-3:2014 | Évaluation biologique des dispositifs médicaux — Partie 3: Essais concernant la génotoxicité, la cancérogénicité et la toxicité sur la reproduction | Standarts spēkā |
| 63448 | ISO 10993-4:2017 | Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood | Standarts spēkā |
| 64750 | ISO 10993-18:2020 | Biological evaluation of medical devices — Part 18: Chemical characterization of medical device materials within a risk management process | Standarts spēkā |
| 75323 | ISO 10993-17:2023 | Biological evaluation of medical devices — Part 17: Toxicological risk assessment of medical device constituents | Standarts spēkā |
| 34213 | ISO 10993-7:2008 | Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals | Standarts spēkā |
| 88201 | ISO 10993-17:2023/Amd 1:2025 | Biological evaluation of medical devices — Part 17: Toxicological risk assessment of medical device constituents — Amendment 1 | Standarts spēkā |
Attēlo no 11. līdz 20. no pavisam 156 ieraksta(-iem).