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aap Implantate AG

DE-MF-000005994 · Germany · Berlin

aap Implantate AG is registered in the European database on medical devices as a manufacturer, with 278 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa200
Class IIb78

Most frequent device types declared: Instrument, Bone plates (non-sterile).

Among these devices, 78 are declared implantable, 200 reusable.

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 entryAAP IMPLANTATE AG (DE) · FDA 8043862
Devices in EUDAMED278
Country of registrationGermany

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