BANDELIN electronic GmbH & Co. KG
DE-MF-000005818 · Germany · Berlin
BANDELIN electronic GmbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 254 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 242 |
|---|
Among these devices, 209 are declared active.
Devices declared under this manufacturer
- DT 156 BH - Version U.K.
- FamoSonic Flush
- IB 20 implant box - 5 pcs.
- K 3 C Einhängekorb
- KT 30 basket holder
- KT 3000 Z R Korbträger
- RK 102 H - BW
- RK 156 BH - Version U.K.
- SONOREX GT 504 M-C
- SONOREX SUPER RK 31
- ST 15.1 - Version U.K.
- ST 514 BH - Version U.K.
Showing 12 of 254 declared devices.
Catalogue references include 1851-GB, 3025-OBL, 3221-GB, 3228, 3284, 3360-FG.
European nomenclature codes declared: Z12011302, W02069080.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 254 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. BANDELIN electronic GmbH & Co. KG was not found in either the U.S. or the Canadian register.