ADEBO Medical & Trade GmbH
DE-MF-000006673 · Germany · Berlin
ADEBO Medical & Trade GmbH is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 6 |
|---|
Most frequent device types declared: Viawant Nitrile Pro.
Devices declared under this manufacturer
- Viawant Nitrile Pro L
- Viawant Nitrile Pro M
- Viawant Nitrile Pro S
- Viawant Nitrile Pro XL
- Viawant Nitrile Pro XS
- Viawant Nitrile Pro XXL
Catalogue references include 60101, 60201, 60301, 60401, 60501, 60601.
European nomenclature codes declared: T01020204.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| 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 | 6 |
|---|---|
| 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. ADEBO Medical & Trade GmbH was not found in either the U.S. or the Canadian register.