EU → US Device Access

Waldemar Knittel Glasbearbeitungs GmbH

DE-MF-000005025 · Germany · Braunschweig

Waldemar Knittel Glasbearbeitungs GmbH is registered in the European database on medical devices as a manufacturer, with 30 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

other30

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 entryWaldemar Knittel Glasbearbeitungs GmbH (DE) · FDA 1000469910
Devices in EUDAMED30
Country of registrationGermany

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