EU → North America Device Access

Moritz Reha-Hilfen GmbH

DE-MF-000005119 · Germany · Wanfried

Moritz Reha-Hilfen GmbH is registered in the European database on medical devices as a manufacturer, with 1 617 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa1 617

Devices declared under this manufacturer

Showing 12 of 1 617 declared devices.

Catalogue references include 10.610-1/30344, 10.610-1/HKM/32364, 10.610-1/HKM/42464, 10.610-5/43435, 10.610-6/38435, 10.621-1/V/60453.

European nomenclature codes declared: V080399, V08030102, Y122499, V080302, V08068099.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED1 617
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 GTIN1 617
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. Moritz Reha-Hilfen GmbH was not found in either the U.S. or the Canadian register.

Other manufacturers in Germany

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