AFNOR - FD CEN/TR 17223
Guidance on the relationship between EN ISO 13485:2016 (Medical devices - Quality management systems - Requirements for regulatory purposes) and European Medical Devices Regulation and In Vitro Diagnostic Medical Devices Regulation
active, Most Current
| Organization: | AFNOR |
| Publication Date: | 14 November 2018 |
| Status: | active |
| ICS Code (Quality management and quality assurance): | 03.120.10 |
| ICS Code (In vitro diagnostic test systems): | 11.100.10 |
| ICS Code (Medical equipment in general): | 11.040.01 |
| ICS Code (Management systems): | 03.100.70 |
Document History
FD CEN/TR 17223
November 14, 2018
Guidance on the relationship between EN ISO 13485:2016 (Medical devices - Quality management systems - Requirements for regulatory purposes) and European Medical Devices Regulation and In Vitro Diagnostic Medical Devices Regulation
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