ISO/TC 210
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 22101 | ISO 13488:1996 | Quality systems Medical devices Particular requirements for the application of ISO 9002 | Atcelts |
| 31349 | ISO 15223:2000 | Medical devices Symbols to be used with medical device labels, labelling and information to be supplied | Atcelts |
| 25799 | ISO 14971-1:1998 | Medical devices Risk management | 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 |
| 55589 | ISO/TS 19218-1:2011 | Medical devices — Hierarchical coding structure for adverse events — Part 1: Event-type codes | 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 |
| 50729 | ISO/IEC Guide 63:2012 | Guide to the development and inclusion of safety aspects in International Standards for medical devices | Atcelts |
| 36029 | ISO 14971:2000/Amd 1:2003 | Medical devices — Application of risk management to medical devices — Amendment 1: Rationale for requirements | 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 |
Displaying 61-70 of 114 results.