Moeck & Moeck GmbH
DE-MF-000007979 · Germany · Hamburg
Moeck & Moeck GmbH is registered in the European database on medical devices as a manufacturer, with 39 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 29 |
|---|---|
| Class IIb | 10 |
Most frequent device types declared: TWINWARM BB, Twinwarm BB 12BB02 (italiano), Twinwarm BB 12BB06 (français), Twinwarm BB 12BB05 (english), Twinwarm BB 12BB01 (deutsch).
Among these devices, 10 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 | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 39 |
| Country of registration | Germany |
⚠️ Absence here is not proof of absence from the market. A manufacturer may reach the United States through a distributor registered under its own name, or under a corporate name we could not match. We publish what we measured, not what we inferred.