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 |
| 45420 | ISO 15223-1:2007/Amd 1:2008 | Medical devices — Symbols to be used with medical device labels, labelling and information to be supplied — Part 1: General requirements — Amendment 1 | 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 |
| 31550 | ISO 14971:2000 | Medical devices — Application of risk management to medical devices | Atcelts |
| 63837 | ISO 80369-20:2015 | Small-bore connectors for liquids and gases in healthcare applications — Part 20: Common test methods | Atcelts |
| 58011 | ISO 80369-7:2016 | Small-bore connectors for liquids and gases in healthcare applications — Part 7: Connectors for intravascular or hypodermic applications | Atcelts |
| 25800 | ISO 14969:1999 | Quality systems — Medical devices — Guidance on the application of ISO 13485 and ISO 13488 | Atcelts |
| 36786 | ISO 13485:2003 | Medical devices — Quality management systems — Requirements for regulatory purposes | Atcelts |
| 62780 | IEC 62366:2007/Amd 1:2014 | Medical devices — Application of usability engineering to medical devices — Amendment 1 | Atcelts |
Displaying 51-60 of 114 results.