VRK Lab GmbH
DE-MF-000010636 · Germany · Stromberg
VRK Lab GmbH is registered in the European database on medical devices as a manufacturer, with 25 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 25 |
|---|
Devices declared under this manufacturer
- Demedent Prophy Powder, cherry
- Demedent Prophy Powder, lemon
- Demedent Prophy Powder, neutral
- Demedent Prophy Powder, strawberry
- Dr. Mayer prophylaxis powder, black currant
- Dr. Mayer prophylaxis powder, cherry
- Dr. Mayer prophylaxis powder, lemon
- Dr. Mayer prophylaxis powder, mint
- Dr. Mayer prophylaxis powder, orange
- Dr. Mayer prophylaxis powder, strawberry
- PROFIFLUSS®CX Complex, lemon
- PROFIFLUSS®CX Complex, mint
Showing 12 of 25 declared devices.
Catalogue references include 032, 034, 073, 074, 075, 076.
European nomenclature codes declared: Q01010403.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 25 |
| 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 | 25 |
|---|---|
| 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. VRK Lab GmbH was not found in either the U.S. or the Canadian register.