ISO/TC 210
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 38594 | IEC 62366:2007 | Medical devices — Application of usability engineering to medical devices | Atcelts |
| 59587 | ISO/TR 24971:2013 | Medical devices — Guidance on the application of ISO 14971 | Atcelts |
| 22101 | ISO 13488:1996 | Quality systems — Medical devices — Particular requirements for the application of ISO 9002 | 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 |
| 38193 | ISO 14971:2007 | Medical devices — Application of risk management to medical devices | Atcelts |
| 63016 | ISO 15225:2016 | Medical devices — Quality management — Medical device nomenclature data structure | 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 |
| 34667 | ISO/TS 20225:2001 | Global medical device nomenclature for the purpose of regulatory data exchange | Atcelts |
| 42342 | ISO 15223-1:2007 | Medical devices — Symbols to be used with medical device labels, labelling and information to be supplied — Part 1: General requirements | Atcelts |
| 67943 | ISO 20417:2021 | Medical devices — Information to be supplied by the manufacturer | Atcelts |
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