ISO/TC 210
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 25800 | ISO 14969:1999 | Quality systems — Medical devices — Guidance on the application of ISO 13485 and ISO 13488 | Atcelts |
| 22101 | ISO 13488:1996 | Quality systems — Medical devices — Particular requirements for the application of ISO 9002 | Atcelts |
| 22101 | ISO 13488:1996 | Quality systems Medical devices Particular requirements for the application of ISO 9002 | Atcelts |
| 59752 | ISO 13485:2016 | Medical devices — Quality management systems — Requirements for regulatory purposes | Standarts spēkā |
| 54724 | ISO 13485:2003/Cor 1:2009 | Medical devices — Quality management systems — Requirements for regulatory purposes — Technical Corrigendum 1 | Atcelts |
| 36786 | ISO 13485:2003 | Medical devices — Quality management systems — Requirements for regulatory purposes | Atcelts |
| 22098 | ISO 13485:1996 | Quality systems Medical devices Particular requirements for the application of ISO 9001 | Atcelts |
| 22098 | ISO 13485:1996 | Quality systems — Medical devices — Particular requirements for the application of ISO 9001 | Atcelts |
| 65624 | IEC/TR 80002-3:2014 | Medical device software — Part 3: Process reference model of medical device software life cycle processes (IEC 62304) | 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 |
Displaying 91-100 of 114 results.