Eckert & Ziegler BEBIG GmbH
Active in EUDAMEDGermanyfrom SRN EUDAMED FDA SRN DE-MF-000005760 FEI 1000310011
- Devices
- 1
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: CE MDR Registry: EUDAMED
Company details
- EUDAMED SRN
- DE-MF-000005760
- FDA FEI number
- 1000310011
- EU VAT number
- DE137169788
- EUDAMED status
- Active
- EUDAMED registered name
- Eckert & Ziegler BEBIG GmbH
- Registered address
- 10, Robert-Rössle-Strasse, D-13125, Berlin, Germany
- Website
- www.bebig.com
- [email protected]
- Phone
- +49 30 941084 0
- PRRC contact
- Bernd Schumacher
Frequently asked questions
How many devices does Eckert & Ziegler BEBIG GmbH have in the registry?
The registry currently lists 1 device for Eckert & Ziegler BEBIG GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eckert & Ziegler BEBIG GmbH's devices?
Among its 1 most recently registered device, Eckert & Ziegler BEBIG GmbH has devices listed in EUDAMED (1 device).
What risk classes do Eckert & Ziegler BEBIG GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Eckert & Ziegler BEBIG GmbH's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Eckert & Ziegler BEBIG GmbH in the registry?
The most recently registered devices listed for Eckert & Ziegler BEBIG GmbH include Safety and Sterilisation Container for Ru-106 Eye Applicators.