CEN/CLC/TC 3
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 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) | |
| 37957 | LVS EN ISO 13485:2016 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) | Standarts spēkā |
| 69481 | LVS EN ISO 13485:2016/A11:2021 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) | Standarts spēkā |
| 64029 | LVS EN ISO 13485:2016/AC:2017 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) | Atcelts |
| 66700 | LVS EN ISO 13485:2016/AC:2018 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) | Standarts spēkā |
| 21479 | LVS 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 | LVS EN ISO 14971:2000/AC:2002 | Medical devices - Application of risk management to medical devices (ISO 14971:2000) | Atcelts |
| 18856 | LVS EN ISO 14971:2003 | Medical devices - Application of risk management to medical devices Medical devices - Application of risk management to medical devices | Atcelts |
| 24162 | LVS EN ISO 14971:2007 | Medical devices - Application of risk management to medical devices | Atcelts |
| 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 91-100 of 139 results.