adeor medical AG
DE-MF-000011451 · Germany · Valley
adeor medical AG is registered in the European database on medical devices as a manufacturer, with 7 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 7 |
|---|
Most frequent device types declared: Meridian Alpha Perforator Ø11/14 mm, 1.0 mm, Meridian Alpha Perforator Ø7/11 mm, 1.0 mm, Meridian Alpha Perforator Ø7/11 mm, 3.0 mm, Meridian Classic Perforator Ø11/14 mm, 2.0 mm, Meridian Classic Perforator Ø8/11 mm, 2.0 mm.
Among these devices, 7 are declared sterile.
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 | ADEOR MEDICAL AG (DE) · FDA 3007031059 |
| Devices in EUDAMED | 7 |
| Country of registration | Germany |
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
MDR-0018 | issued | 2029-10-15 |