Eckert & Ziegler BEBIG GmbH
DE-MF-000005760 · Germany · Berlin
Eckert & Ziegler BEBIG GmbH is registered in the European database on medical devices as a manufacturer, with 26 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 13 |
|---|---|
| Class IIb | 13 |
Among these devices, 12 are declared reusable, 13 active.
Devices declared under this manufacturer
- Dummy, silver, type CCA
- Dummy, silver, type CCC
- Dummy, silver, type CIA
- Dummy, silver, type COB
- Dummy, silver, type COC
- Dummy, silver, type COE
- Ru-106 Eye Applicator, type CCA
- Ru-106 Eye Applicator, type CCC
- Ru-106 Eye Applicator, type CCD
- Ru-106 Eye Applicator, type CCX
- Ru-106 Eye Applicator, type CGD
- Ru-106 Eye Applicator, type COC
Showing 12 of 26 declared devices.
Catalogue references include AGD.A24, AGD.A28, AGD.A31, AGD.A33, Ru6.A03, Ru6.A07.
European nomenclature codes declared: Z11010385.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | ECKERT & ZIEGLER BEBIG GMBH (DE) · FDA 9617477 |
| Devices in EUDAMED | 26 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 26 |
|---|---|
| Found in the U.S. device database | 25 |
| Share | 96.2 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | ECKERT & ZIEGLER BEBIG, INC. |
North American profile: Both markets. Eckert & Ziegler BEBIG GmbH is registered in both the United States and Canada.