TBF GlobalMed. GmbH
DE-MF-000042609 · Germany · Frankfurt am Main
TBF GlobalMed. GmbH is registered in the European database on medical devices as a manufacturer, with 84 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 84 |
|---|
Among these devices, 84 are declared sterile.
Devices declared under this manufacturer
- FATS
- LUCIDUS HA
- Q02030301
- VISCO HYL
- ZenoSight
Showing 12 of 84 declared devices.
Catalogue references include LUCA2030, VISA2018, VISA2030, VISA3020, ZENA1010, ZENA1016.
European nomenclature codes declared: Q02030301.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 84 |
| 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 | 84 |
|---|---|
| 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. TBF GlobalMed. GmbH was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
6QMS-MDR-0075/07/2025 | issued | 2030-07-01 |