ISO/TC 210
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 59752 | ISO 13485:2016 | Medical devices — Quality management systems — Requirements for regulatory purposes | Standarts spēkā |
| 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 |
| 25800 | ISO 14969:1999 | Quality systems — Medical devices — Guidance on the application of ISO 13485 and ISO 13488 | Atcelts |
| 25799 | ISO 14971-1:1998 | Medical devices — Risk management — Part 1: Application of risk analysis | Atcelts |
| 25799 | ISO 14971-1:1998 | Medical devices Risk management | Atcelts |
| 31550 | ISO 14971:2000 | Medical devices — Application of risk management to 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 |
| 38193 | ISO 14971:2007 | Medical devices — Application of risk management to medical devices | Atcelts |
| 72704 | ISO 14971:2019 | Medical devices — Application of risk management to medical devices | Standarts spēkā |
Displaying 21-30 of 114 results.