FBI Medizintechnik GmbH
DE-MF-000024110 · Germany · Taufkirchen
FBI Medizintechnik GmbH is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 5 |
|---|
Devices declared under this manufacturer
- Bite guard for single use
- EEG/EMG/ECG liquid gel electrode for ECT monitoring
- Single Electrode Connection Cable Set of 2 (long)
- Single Electrode Connection Cable Set of 5
- Single Electrode Connection Cable Set of 9
Catalogue references include BIGU-S, EEDS-LG, ELDW-2, ELDW-5, ELDW-9.
European nomenclature codes declared: N0199, G030804, N010180.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 5 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 5 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
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. FBI Medizintechnik GmbH was not found in either the U.S. or the Canadian register.