Renfert GmbH
DE-MF-000005448 · Germany · Hilzingen
Renfert GmbH is registered in the European database on medical devices as a manufacturer, with 14 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 14 |
|---|
Most frequent device types declared: Sympro.
Among these devices, 5 are declared active.
No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | RENFERT GMBH (DE) · FDA 3001065024 |
| Devices in EUDAMED | 14 |
| Country of registration | Germany |