BENTEC Endoscopy GmbH

Country not established FDA FEI 1000343527

Devices: 0
Registrations: FDA
FDA recalls: 0

No devices from this company are in the catalogue yet.

At a glance

Counted by deviCERTS from registry records

Market reach

United States: FDA FEI

Company details

FDA FEI number: 1000343527
Address: Hinteres Oeschle 6, Rietheim-Weilheim Baden-Wurttemberg