EU → North America Device Access

Med Auxil analysis aids e.K.

DE-MF-000027810 · Germany · Seesen

Med Auxil analysis aids e.K. is registered in the European database on medical devices as a manufacturer, with 11 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Devices declared under this manufacturer

Catalogue references include 01.002, 25.016, 25.017, 4262389480149, 50004, Fecescatcher.

European nomenclature codes declared: W050180.

United States market access

FDA establishment registerRegistered with FDA
Matched entryMED AUXIL ANALYSIS AIDS E.K. (DE) · FDA 3030125016
Devices in EUDAMED11
Country of registrationGermany

Device-level evidence

Devices with a numeric GTIN11
Found in the U.S. device database1
Share9.1 %

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. Med Auxil analysis aids e.K. is registered in the United States but was not found in the Canadian register.

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