ISO/TC 210
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 72042 | IEC 62366-1:2015/Cor 1:2016 | Medical devices — Part 1: Application of usability engineering to medical devices — Technical Corrigendum 1 | Standarts spēkā |
| 60044 | ISO/TR 80002-2:2017 | Medical device software — Part 2: Validation of software for medical device quality systems | Standarts spēkā |
| 54146 | IEC/TR 80002-1:2009 | Medical device software — Part 1: Guidance on the application of ISO 14971 to medical device software | Standarts spēkā |
| 36029 | ISO 14971:2000/Amd 1:2003 | Medical devices — Application of risk management to medical devices — Amendment 1: Rationale for requirements | Atcelts |
| 50729 | ISO/IEC Guide 63:2012 | Guide to the development and inclusion of safety aspects in International Standards for medical devices | Atcelts |
| 22098 | ISO 13485:1996 | Quality systems Medical devices Particular requirements for the application of ISO 9001 | Atcelts |
| 38062 | ISO 15223:2000/Amd 2:2004 | Medical devices — Symbols to be used with medical device labels, labelling and information to be supplied — Amendment 2 | Atcelts |
| 38594 | IEC 62366:2007 | Medical devices — Application of usability engineering to medical devices | Atcelts |
| 34667 | ISO/TS 20225:2001 | Global medical device nomenclature for the purpose of regulatory data exchange | Atcelts |
| 55589 | ISO/TS 19218-1:2011 | Medical devices — Hierarchical coding structure for adverse events — Part 1: Event-type codes | Atcelts |
Displaying 31-40 of 114 results.