EU → North America Device Access

Bauerfeind AG

DE-MF-000007543 · Germany · Zeulenroda-Triebes

Bauerfeind AG is registered in the European database on medical devices as a manufacturer, with 36 507 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa36 507

Devices declared under this manufacturer

Showing 12 of 36 507 declared devices.

Catalogue references include 20760725500009, 20762025420334, 20780421720223, 20780431200331, 21260711420224, 21264714224323.

European nomenclature codes declared: M030405, Y061209, Y06120601, Y061203, Y060615, Y060308.

United States market access

FDA establishment registerRegistered with FDA
Matched entryBAUERFEIND AG (DE) · FDA 8010507
Devices in EUDAMED36 507
Country of registrationGermany

Device-level evidence

Devices with a numeric GTIN36 507
Found in the U.S. device database20 554
Share56.3 %

Canadian market access

Health Canada licence listingLicensed in Canada
Matched entryBAUERFEIND AG

North American profile: Both markets. Bauerfeind AG is registered in both the United States and Canada.

Other manufacturers in Germany

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