EU → US Device Access

WiMedical GmbH

DE-MF-000036069 · Germany · Singen (Hohentwiel)

WiMedical GmbH is registered in the European database on medical devices as a manufacturer, with 41 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa41

Most frequent device types declared: 56er-1/1-BIG-Boden-FG-Drahtsieb, 56er-1/1-Boden-FG-Hybrid, 56er-1/2-Boden-FG-Drahtsieb, 106er-1/2-Boden-FG-Edelstahl, 56er-1/2-Boden-FG-Edelstahl.

Among these devices, 40 are declared 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 registerNot found in the FDA register
Devices in EUDAMED41
Country of registrationGermany
⚠️ Absence here is not proof of absence from the market. A manufacturer may reach the United States through a distributor registered under its own name, or under a corporate name we could not match. We publish what we measured, not what we inferred.

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