DB Biotech, a.s.
SK-MF-000051838 · Slovakia · Košice
DB Biotech, a.s. is registered in the European database on medical devices as a manufacturer, with 360 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: DB 038, DB 051, DB 061, DB 082, DB 119.
Devices declared under this manufacturer
- Anti-BRAF
- Anti-CD3
- Anti-CD34
- Anti-Chromogranin A
- Anti-Cytokeratin 20
- Anti-Cytokeratin 7
- Anti-Cytokeratin 8
- Anti-EBV/LMP-1
- Anti-Human IgG
- Anti-Human Kappa Light Chain
- Anti-Human SOX10
- Anti-Napsin A
Showing 12 of 360 declared devices.
Catalogue references include DB 038-0.2, DB 051-0.2, DB 061-0.2, DB 151-RTU-15, DB 159-RTU-15, DB 174-0.5.
European nomenclature codes declared: W01030705, W01030799, W01030706.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 360 |
| Country of registration | Slovakia |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 360 |
|---|---|
| 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. DB Biotech, a.s. was not found in either the U.S. or the Canadian register.