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 |
| 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 |
| 31550 | ISO 14971:2000 | Medical devices — Application of risk management to medical devices | Atcelts |
| 36786 | ISO 13485:2003 | Medical devices — Quality management systems — Requirements for regulatory purposes | Atcelts |
| 45976 | ISO 80369-1:2010 | Small-bore connectors for liquids and gases in healthcare applications — Part 1: General requirements | Atcelts |
| 50734 | ISO 80369-6:2016 | Small bore connectors for liquids and gases in healthcare applications — Part 6: Connectors for neuraxial applications | Atcelts |
Displaying 61-70 of 114 results.