BioSciTec GmbH
DE-MF-000007888 · Germany · Frankfurt am Main
BioSciTec GmbH is registered in the European database on medical devices as a manufacturer, with 11 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: mB2.
Devices declared under this manufacturer
- BLOTrix System 4/ BLOTrix Reader C1
- BLOTrix System 4/ BLOTrix Reader C1 L
- BLOTrix System 4/ BLOTrix Reader R2 L
- BLOTrix System 4/ BLOTrix Reader S1
- BLOTrix System 5/ BLOTrix Reader C1 L
- BLOTrix System 5/ BLOTrix Reader R2 L
- BLOTrix System 5/ BLOTrix Reader S1
- JAEGER mobile Reader
- recomScan System 5/ BLOTrix Reader C1 L
- recomScan System 5/ BLOTrix Reader R2 L
- recomScan System 5/ BLOTrix Reader S1
Catalogue references include b4c4btrc1, b4c4btrc1l, b4c4btrr2l, b55btrc1l, b55btrs1, rs55btrc1l.
European nomenclature codes declared: W0201069080.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 11 |
| 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 | 11 |
|---|---|
| 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. BioSciTec GmbH was not found in either the U.S. or the Canadian register.