MDCG guidance
Guidance on medical devices, active implantable medical devices and in vitro diagnostic medical devices in the COVID-19 context
MDCG guidance · COVID-19 · April 2020
Key facts
| Reference | Guidance on medical devices, active implantable medical devices and in vitro diagnostic medical devices in the COVID-19 context |
|---|---|
| Title | Guidance on medical devices, active implantable medical devices and in vitro diagnostic medical devices in the COVID-19 context |
| Topic | COVID-19 |
| Published | April 2020 |
| Document | health.ec.europa.eu |
At a glance
- Yes Full text searchable in Orca1
- Guidance on medical devices, active implantable medical devices and in vitro diagnostic medical devices in the COVID-19 context Revisions on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About MDCG guidance documents
The Medical Device Coordination Group (MDCG), made up of EU member-state experts, endorses guidance on applying the Medical Devices Regulation (EU) 2017/745 and the In Vitro Diagnostic Regulation (EU) 2017/746. Each page here covers one document and all of its revisions.