ISO/TC 210
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 33753 | ISO/TS 19218:2005 | Medical devices — Coding structure for adverse event type and cause | Atcelts |
| 34667 | ISO/TS 20225:2001 | Global medical device nomenclature for the purpose of regulatory data exchange | Atcelts |
| 36029 | ISO 14971:2000/Amd 1:2003 | Medical devices — Application of risk management to medical devices — Amendment 1: Rationale for requirements | Atcelts |
| 36257 | ISO 15225:2000/Amd 1:2004 | Nomenclature — Specification for a nomenclature system for medical devices for the purpose of regulatory data exchange — Amendment 1 | Atcelts |
| 36786 | ISO 13485:2003 | Medical devices — Quality management systems — Requirements for regulatory purposes | 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 |
| 38193 | ISO 14971:2007 | Medical devices — Application of risk management to medical devices | Atcelts |
| 38194 | ISO/PWI 14971-B | Medical devices — Application of risk management to medical devices — Part B: In vitro diagnostic medical devices | Izstrādē |
| 38401 | ISO/TR 16142:2006 | Medical devices — Guidance on the selection of standards in support of recognized essential principles of safety and performance of medical devices | Atcelts |
| 38421 | IEC 62304:2006 | Medical device software — Software life cycle processes | Standarts spēkā |
Displaying 21-30 of 114 results.