Petermann GmbH
DE-MF-000013598 · Germany · Dombühl
Petermann GmbH is registered in the European database on medical devices as a manufacturer, with 153 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 153 |
|---|
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 | Petermann GmbH (DE) · FDA 9615109 |
| Devices in EUDAMED | 153 |
| Country of registration | Germany |