CEN/CLC/TC 3
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 38201 | LVS EN ISO 13485:2012 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003) | |
| 38201 | EN ISO 13485:2012 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003) | Atcelts |
| 37957 | LVS EN ISO 13485:2016 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) | Standarts spēkā |
| 37957 | EN ISO 13485:2016 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) | Standarts spēkā |
| 33578 | EN ISO 13485:2003/AC:2009 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003/Cor 1:2009) | Atcelts |
| 33578 | LVS EN ISO 13485:2003 /AC:2010 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003/Cor 1:2009) | Atcelts |
| 32600 | EN 15986:2011 | Symbol for use in the labelling of medical devices - Requirements for labelling of medical devices containing phthalates | Izstrādē |
| 32600 | LVS EN 15986:2011 | Symbol for use in the labelling of medical devices - Requirements for labelling of medical devices containing phthalates | Standarts spēkā |
| 32013 | prEN ISO 13485 rev | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003) | Izstrādē |
| 32012 | LVS EN ISO 14971:2009 | Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01) | Atcelts |
Displaying 81-90 of 144 results.