CEN/CLC/TC 3
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 39198 | EN 1041:2008/FprA1 | Information supplied by the manufacturer of medical devices | Izstrādē |
| 38595 | LVS EN ISO 14971:2012 | 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 |
| 38536 | LVS EN ISO 13485:2012/AC:2012 | Medical devices - Quality management systems - Requirements for regulatory purposes - Technical Corrigendum 1 (ISO 13485:2003+Cor 1:2009) | |
| 38536 | EN ISO 13485:2012/AC:2012 | Medical devices - Quality management systems - Requirements for regulatory purposes - Technical Corrigendum 1 (ISO 13485:2003+Cor 1:2009) | Atcelts |
| 38201 | EN ISO 13485:2012 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003) | Atcelts |
| 38201 | LVS EN ISO 13485:2012 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003) | |
| 37957 | EN ISO 13485:2016 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) | Standarts spēkā |
| 37957 | LVS EN ISO 13485:2016 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) | Standarts spēkā |
| 33578 | LVS EN ISO 13485:2003 /AC:2010 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003/Cor 1:2009) | Atcelts |
Displaying 71-80 of 139 results.