ISO/TC 210
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 67942 | ISO/TR 20416:2020 | Medical devices — Post-market surveillance for manufacturers | Standarts spēkā |
| 59587 | ISO/TR 24971:2013 | Medical devices — Guidance on the application of ISO 14971 | Atcelts |
| 74437 | ISO/TR 24971:2020 | Medical devices — Guidance on the application of ISO 14971 | Standarts spēkā |
| 60044 | ISO/TR 80002-2:2017 | Medical device software — Part 2: Validation of software for medical device quality systems | Standarts spēkā |
| 69336 | ISO/TS 11633-1:2019 | Health informatics — Information security management for remote maintenance of medical devices and medical information systems — Part 1: Requirements and risk analysis | Standarts spēkā |
| 55589 | ISO/TS 19218-1:2011 | Medical devices — Hierarchical coding structure for adverse events — Part 1: Event-type codes | Atcelts |
| 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 |
| 33753 | ISO/TS 19218:2005 | Medical devices — Coding structure for adverse event type and cause | Atcelts |
| 55590 | ISO/TS 19218-2:2012 | Medical devices — Hierarchical coding structure for adverse events — Part 2: Evaluation codes | Atcelts |
| 34667 | ISO/TS 20225:2001 | Global medical device nomenclature for the purpose of regulatory data exchange | Atcelts |
Displaying 101-110 of 114 results.