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Gimmi GmbH

DE-MF-000005445 · Germany · Tuttlingen

Gimmi GmbH is registered in the European database on medical devices as a manufacturer, with 2 741 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa2 741

Among these devices, 2 260 are declared reusable, 10 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 registerRegistered with FDA
Matched entryGIMMI GMBH (DE) · FDA 9612074
Devices in EUDAMED2 741
Country of registrationGermany

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