Kommanditgesellschaft Behnk Elektronik GmbH & Co.
DE-MF-000005304 · Germany · Norderstedt
Kommanditgesellschaft Behnk Elektronik GmbH & Co. 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
Most frequent device types declared: Cuvettes and balls, Thrombo C, Thrombolyzer, Thrombomate, Thrombostat.
Devices declared under this manufacturer
- BE Clean Pro
- Balls
- Behnk
- Cuvettes and balls
- Cuvettes for predilution
- LTA Reagenz SPA 0.9
- Predilution bar B
- Sample tubes
- Thrombolyzer XR
- Thrombolyzer XRM
- Thrombolyzer cuvette racks
- Thrombostat +
Showing 12 of 35 declared devices.
Catalogue references include 018012, 050150, 050220, 050280, 050951, 057660.
European nomenclature codes declared: W0202020185, W0202020101, W0202020102, W0202029085, W0202020180, W01030299.
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.
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | KOMMANDITGESELLSCHAFT BEHNK ELEKTRONIK GMBH & CO. |
North American profile: Canada only. Kommanditgesellschaft Behnk Elektronik GmbH & Co. holds a Canadian licence but was not found in the U.S. register.