CEN/CLC/TC 3
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 69481 | EN ISO 13485:2016/A11:2021 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) | Standarts spēkā |
| 64029 | EN ISO 13485:2016/AC:2016 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) | Atcelts |
| 66700 | EN ISO 13485:2016/AC:2018 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) | Izstrādē |
| 18856 | EN ISO 14971:2000 | Medical devices - Application of risk management to medical devices (ISO 14971:2000) | Atcelts |
| 21479 | EN ISO 14971:2000/A1:2003 | Medical devices - Application of risk management to medical devices - Amendment 1: Rationale for requirements (ISO 14971:2000/AM1:2003) | Atcelts |
| 21072 | EN ISO 14971:2000/AC:2002 | Medical devices - Application of risk management to medical devices (ISO 14971:2000) | Atcelts |
| 24162 | EN ISO 14971:2007 | Medical devices - Application of risk management to medical devices (ISO 14971:2007) | Atcelts |
| 32012 | EN ISO 14971:2009 | Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01) | Atcelts |
| 38595 | EN ISO 14971:2012 | Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01) | Atcelts |
| 63920 | EN ISO 14971:2019 | Medical devices - Application of risk management to medical devices (ISO 14971:2019) | Standarts spēkā |
Displaying 31-40 of 139 results.