EU → North America Device Access

BEKA-Hospitec GmbH

DE-MF-000013895 · Germany · Wetzlar

BEKA-Hospitec GmbH is registered in the European database on medical devices as a manufacturer, with 598 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa598

Most frequent device types declared: K101 BEKA Pflege- und Versorgungsliegen und deren Zubehöre, K109 BEKA Hydrotherapie Produkte und deren Zubehör, K119 BEKA Gurte – Lifter Zubehöre, K120 BEKA Lifter und deren Zubehör, K121 BEKA Dusch- und Badelifter und deren Zubehöre.

Among these devices, 430 are declared active.

Devices declared under this manufacturer

Showing 12 of 598 declared devices.

Catalogue references include K109 BEKA Hydrotherapie Produkte und deren Zubehör, K119 BEKA Gurte – Lifter Zubehöre, K120 BEKA Lifter / Aufstehhilfe und deren Zubehör, K120 BEKA Lifter und deren Zubehör, K121 BEKA Dusch- und Badelifter und deren Zubehöre, K122 BEKA Pflegebadewannen und deren Zubehör.

European nomenclature codes declared: Y093399, V0805038002, V0805030102, Y1803, Y093312, V08050303.

United States market access

FDA establishment registerRegistered with FDA
Matched entryBEKA Hospitec GMBH (DE) · FDA 3003878287
Devices in EUDAMED598
Country of registrationGermany

Device-level evidence

Devices with a numeric GTIN598
Found in the U.S. device database39
Share6.5 %

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. BEKA-Hospitec GmbH is registered in the United States but was not found in the Canadian register.

Other manufacturers in Germany

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