VIOMED Vertriebs GmbH
DE-MF-000043019 · Germany · Kloster Lehnin
VIOMED Vertriebs 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 |
|---|
Devices declared under this manufacturer
- restifem Medium
- restifem Set
- restifem Small
- restifem pro Large
- restifem pro Medium
- restifem pro Small
Catalogue references include R011M, R011S, R011Set, Rpro011L, Rpro011M, Rpro011S.
European nomenclature codes declared: U089005.
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. VIOMED Vertriebs GmbH was not found in either the U.S. or the Canadian register.