CEN/CLC/TC 3
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 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 |
| 33578 | EN ISO 13485:2003/AC:2009 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003/Cor 1:2009) | Atcelts |
| 24838 | EN 1041:2008 | Information supplied by the manufacturer of medical devices | Atcelts |
| 22133 | EN ISO 13485:2003 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003) | Atcelts |
| 24766 | EN 980:2008 | Symbols for use in the labelling of medical devices | Atcelts |
| 26098 | EN 15546-1:2008 | Small bore connectors for liquids and gases in healthcare applications - Part 1 - General Requirements | Atcelts |
| 38201 | EN ISO 13485:2012 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003) | Atcelts |
| 32012 | EN ISO 14971:2009 | Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01) | Atcelts |
| 21072 | LVS EN ISO 14971:2000/AC:2002 | Medical devices - Application of risk management to medical devices (ISO 14971:2000) | Atcelts |
| 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 |
Displaying 91-100 of 141 results.