EU → North America Device Access

Fuhrmann GmbH

DE-MF-000006652 · Germany · Much

Fuhrmann GmbH is registered in the European database on medical devices as a manufacturer, with 1 019 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa1 019

Most frequent device types declared: Bauchtücher, Binden und Verbände, Einmalinstrumente Magillzangen, Einmalinstrumente Nadelhalter, Mullkompressen mit Röntgenkontrast.

Among these devices, 577 are declared sterile.

Devices declared under this manufacturer

Showing 12 of 1 019 declared devices.

Catalogue references include 29072, 31131, 31189, 31251, 31424, 32036.

European nomenclature codes declared: M020199, V9012, M0201050101, M0201020201, M0304010102, M0201030201.

United States market access

FDA establishment registerRegistered with FDA
Matched entryFUHRMANN GMBH (DE) · FDA 3013118873
Devices in EUDAMED1 019
Country of registrationGermany

Device-level evidence

Devices with a numeric GTIN1 019
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: United States only. Fuhrmann GmbH is registered in the United States but was not found in the Canadian register.

Other manufacturers in Germany

All Germany manufacturers →