LABiTec LAbor BioMedical Technologies GmbH
DE-MF-000020928 · Germany · Ahrensburg
LABiTec LAbor BioMedical Technologies GmbH is registered in the European database on medical devices as a manufacturer, with 14 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: CD12-1-17.
Devices declared under this manufacturer
- CA-101
- CoaDATA 2004
- CoaDATA 4004
- CoaDATA 504
- CoaDATA 504+
- DCA-1+
- DCA-2
- DCA-4
- Thrombo Fast +
- Thrombo Speedy +
- biobas 10
- biobas 20
Showing 12 of 14 declared devices.
Catalogue references include 105-99-150-00, 112-99-090-00, 112-99-130-00, 112-99-320-00, 112-99-340-00, 112-99-520-00.
European nomenclature codes declared: W0202020101.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 14 |
| 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 | 14 |
|---|---|
| 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. LABiTec LAbor BioMedical Technologies GmbH was not found in either the U.S. or the Canadian register.