VELLAP Diagnostics GmbH
DE-MF-000035636 · Germany · Weimar
VELLAP Diagnostics GmbH is registered in the European database on medical devices as a manufacturer, with 35 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- Cleartest Albu-Mic
- Cleartest Cardio Rapid
- Cleartest D-Dimer
- Cleartest Humanofecal
- Cleartest TSH
- Cleartest Troponin I Infarkt
- IDEAL Influenza A+B
- TOP Albu-Mic
- TOP D-Dimer
- TOP Humanofecal
- VELLAP D-Dimer
- VELLAP FOB
Showing 12 of 35 declared devices.
Catalogue references include 2.13.6.11, 2.13.6.12, 2.13.6.2, 2.13.6.3, C3 0501-5-MTU, C3 0501-E.
European nomenclature codes declared: W01021306, W0105011101, W0103020503, W0102039013, W0105040604, W01010201.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 35 |
| 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 | 35 |
|---|---|
| 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. VELLAP Diagnostics GmbH was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
IX 2512862-2 | issued | 2030-07-23 |
IX 2512862-1 | issued | 2030-07-23 |
HX 2512862-1 | issued | 2030-07-23 |