ADODERM GMBH
DE-MF-000005720 · Germany · Köln
ADODERM GMBH is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class I | 8 |
|---|
Among these devices, 8 are declared sterile, 8 implantable.
Devices declared under this manufacturer
- HYABELL®
- VARIODERM ®
- VARIOFILL®
Catalogue references include HBB16, HBD20, HBL12, HBM12, HBU24, VBC.
European nomenclature codes declared: P900402.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 8 |
| 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 | 8 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | ADODERM GMBH |
North American profile: Canada only. ADODERM GMBH holds a Canadian licence but was not found in the U.S. register.