ISO/TC 210
| Reģistrācijas numurs (WIID) | Projekta Nr. | Nosaukums | Statuss |
|---|---|---|---|
| 67284 | ISO 18250-1:2018 | Medical devices — Connectors for reservoir delivery systems for healthcare applications — Part 1: General requirements and common test methods | Standarts spēkā |
| 54146 | IEC/TR 80002-1:2009 | Logiciels de dispositifs médicaux — Partie 1: Titre manque | Standarts spēkā |
| 60044 | ISO/TR 80002-2:2017 | Medical device software — Part 2: Validation of software for medical device quality systems | Standarts spēkā |
| 67942 | ISO/TR 20416:2020 | Medical devices — Post-market surveillance for manufacturers | Standarts spēkā |
| 58085 | ISO/TS 19218-1:2011/Amd 1:2013 | Medical devices — Hierarchical coding structure for adverse events — Part 1: Event-type codes — Amendment 1 | Atcelts |
| 36029 | ISO 14971:2000/Amd 1:2003 | Dispositifs médicaux — Application de la gestion des risques aux dispositifs médicaux — Amendement 1: Justification des exigences | Atcelts |
| 50729 | ISO/IEC Guide 63:2012 | Guide to the development and inclusion of safety aspects in International Standards for medical devices | Atcelts |
| 38062 | ISO 15223:2000/Amd 2:2004 | Dispositifs médicaux — Symboles à utiliser avec les étiquettes, l'étiquetage et les informations à fournir relatifs aux dispositifs médicaux — Amendement 2 | Atcelts |
| 22098 | ISO 13485:1996 | Kvalitātes sistēmas - Medicīniskās ierīces - Īpašas prasības ISO 9001 lietošanai | Atcelts |
| 30163 | ISO/TR 16142:1999 | Medical devices — Guidance on the selection of standards in support of recognized essential principles of safety and performance of medical devices | Atcelts |
Attēlo no 31. līdz 40. no pavisam 114 ieraksta(-iem).