Richard Cermak Minitaschenlampen Inh. Sven Cermak e.K.
DE-MF-000006295 · Germany · Pforzheim
Richard Cermak Minitaschenlampen Inh. Sven Cermak e.K. is registered in the European database on medical devices as a manufacturer, with 17 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 17 |
|---|
Most frequent device types declared: NOVA.
Among these devices, 17 are declared active.
Devices declared under this manufacturer
- CE-Light
- LUNA
- LUX
- MAGIC
- NOVA
Showing 12 of 17 declared devices.
Catalogue references include CE250D, LU300D, LX200D, LX210D, LX210DW, MA350DW.
European nomenclature codes declared: Z12040199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 17 |
| 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 | 17 |
|---|---|
| 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. Richard Cermak Minitaschenlampen Inh. Sven Cermak e.K. was not found in either the U.S. or the Canadian register.