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 IIa | 598 |
|---|
Most frequent device types declared: K122 BEKA Pflegebadewannen und deren Zubehör, K119 BEKA Gurte – Lifter Zubehöre, K120 BEKA Lifter und deren Zubehör, K126 BEKA Pflege- und Versorgungsliegen und deren Zubehör, K121 BEKA Dusch- und Badelifter und deren Zubehöre.
Among these devices, 430 are declared active.
No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | BEKA Hospitec GMBH (DE) · FDA 3003878287 |
| Devices in EUDAMED | 598 |
| Country of registration | Germany |