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AKTORmed GmbH

DE-MF-000006136 · Germany · Neutraubling

AKTORmed GmbH is registered in the European database on medical devices as a manufacturer, with 49 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa49

Among these devices, 40 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 registerRegistered with FDA
Matched entryAKTORmed GmbH (DE) · FDA 3011390076
Devices in EUDAMED49
Country of registrationGermany

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