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Friedrich Bosch GmbH&Co.KG

DE-MF-000005955 · Germany · Bisingen

Friedrich Bosch GmbH&Co.KG is registered in the European database on medical devices as a manufacturer, with 165 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa165

Most frequent device types declared: F BOSCH INFUSION CUFF.

Among these devices, 165 are declared with a measuring function.

Devices declared under this manufacturer

Showing 12 of 165 declared devices.

Catalogue references include 9011.20.169, 9011.21.116, 9011.21.162, 9011.30.162, 9021.20.019, 9022.20.112.

European nomenclature codes declared: C9006, Z12030399.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED165
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 GTIN165
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. Friedrich Bosch GmbH&Co.KG was not found in either the U.S. or the Canadian register.

Other manufacturers in Germany

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