EU → North America Device Access

Rehastage GmbH

DE-MF-000009450 · Germany · Quakenbrück

Rehastage GmbH is registered in the European database on medical devices as a manufacturer, with 12 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa12

Most frequent device types declared: Badewannengriff HUGO, Bett Aufsteh- und Aufrichthilfe TRUDI, Bettgriff Frida, Greifzange Falke, Strumpfanziehhilfe \.

Devices declared under this manufacturer

Catalogue references include BETTG010, FALKE060, FALKE060P, FALKE078L, FRIDOLIN 010, FROTI010.

European nomenclature codes declared: Y242103, Y181806, Y99.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED12
Country of registrationGermany

⚠️ Not found is not the same as not sold — how this comparison can be wrong.

Device-level evidence

Devices with a numeric GTIN12
Found in the U.S. device database0
Share0.0 %

Canadian market access

Health Canada licence listingNot found in the Canadian register

⚠️ Canada lists no Class I devices at all — what that excludes.

North American profile: Neither register. Rehastage GmbH was not found in either the U.S. or the Canadian register.

Other manufacturers in Germany

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