Viromed Medical AG
DE-MF-000047406 · Germany · Rellingen
Viromed Medical AG 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 IIa | 8 |
|---|
Most frequent device types declared: 140.
Among these devices, 3 are declared sterile, 6 active.
Devices declared under this manufacturer
- RUCK ViroCAP Kaltplasma Einweg-Spacer, unsteril, 12 Stück
- RUCK ViroCap Kaltplasma
- ViroCAP derma
- ViroCAP derma Spacer
- ViroCAP derma Spacer 1x
- ViroCAP med
- ViroCAP med Spacer
- ViroCAP med Spacer 1x
Catalogue references include 1310001, 1310101, 140, 144, 151, 152.
European nomenclature codes declared: V9099, Z12019003.
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 | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. Viromed Medical AG was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
MDR 824234 | issued | 2031-07-05 |