ISO/TC 210
| Reģistrācijas numurs (WIID) | Projekta Nr. | Nosaukums | Statuss |
|---|---|---|---|
| 72704 | ISO 14971:2019 | Medical devices — Application of risk management to medical devices | Standarts spēkā |
| 38421 | IEC 62304:2006 | Logiciels de dispositifs médicaux — Processus du cycle de vie du logiciel | Standarts spēkā |
| 65624 | IEC/TR 80002-3:2014 | Medical device software — Part 3: Process reference model of medical device software life cycle processes (IEC 62304) | Standarts spēkā |
| 72042 | IEC 62366-1:2015/Cor 1:2016 | Dispositifs médicaux — Partie 1: Application de l'ingénierie de l'aptitude à l'utilisation aux dispositifs médicaux — Rectificatif technique 1 | Standarts spēkā |
| 85462 | ISO 80369-6:2025 | Small bore connectors for liquids and gases in healthcare applications — Part 6: Connectors for neural applications | Standarts spēkā |
| 67943 | ISO 20417:2021 | Medical devices — Information to be supplied by the manufacturer | Standarts spēkā |
| 63179 | IEC 62366-1:2015 | Medical devices — Part 1: Application of usability engineering to medical devices | Standarts spēkā |
| 61895 | ISO 18250-3:2018 | Medical devices — Connectors for reservoir delivery systems for healthcare applications — Part 3: Enteral applications | Standarts spēkā |
| 74038 | ISO 80369-3:2016/Amd 1:2019 | Small-bore connectors for liquids and gases in healthcare applications — Part 3: Connectors for enteral applications — Amendment 1 | Standarts spēkā |
| 67942 | ISO/TR 20416:2020 | Medical devices — Post-market surveillance for manufacturers | Standarts spēkā |
Attēlo no 101. līdz 110. no pavisam 114 ieraksta(-iem).