ISO/TC 210
| Reģistrācijas numurs (WIID) | Projekta Nr. | Nosaukums | Statuss |
|---|---|---|---|
| 59752 | ISO 13485:2016 | Medical devices — Quality management systems — Requirements for regulatory purposes | Standarts spēkā |
| 64686 | IEC 62304:2006/Amd 1:2015 | Logiciels de dispositifs médicaux — Processus du cycle de vie du logiciel — Amendement 1 | Standarts spēkā |
| 74437 | ISO/TR 24971:2020 | Dispositifs médicaux — Recommandations relatives à l'application de l'ISO 14971 | Standarts spēkā |
| 63179 | IEC 62366-1:2015 | Medical devices — Part 1: Application of usability engineering to medical devices | Standarts spēkā |
| 42343 | ISO 15223-2:2010 | Medicīniskās ierīces. Medicīnisko ierīču etiķešu simboli, marķēšana un pavadinformācija. 2.daļa: Simbolu izstrāde, izvēle un validācija | Standarts spēkā |
| 69126 | IEC/TR 62366-2:2016 | Dispositifs médicaux — Partie 2: Titre manque | Standarts spēkā |
| 88714 | ISO 20417:2026 | Medical devices — Information to be supplied by the manufacturer | Standarts spēkā |
| 60044 | ISO/TR 80002-2:2017 | Medical device software — Part 2: Validation of software for medical device quality systems | Standarts spēkā |
| 72704 | ISO 14971:2019 | Medical devices — Application of risk management to medical devices | Standarts spēkā |
| 86270 | ISO 15223-1:2021/Amd 1:2025 | Medical devices — Symbols to be used with information to be supplied by the manufacturer — Part 1: General requirements — Amendment 1: Addition of defined term for authorized representative and modified EC REP symbol to not be country or region specific | Standarts spēkā |
Attēlo no 101. līdz 110. no pavisam 115 ieraksta(-iem).