NEUROMED
FR-MF-000028522 · France · ENTRAIGUES SUR LA SORGUE
NEUROMED is registered in the European database on medical devices as a manufacturer, with 13 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIa | 13 |
|---|
Most frequent device types declared: NM-G034.02-01, Neuron-Spectrum.
Among these devices, 11 are declared active.
Devices declared under this manufacturer
- Evidence EEG61
- Evidence EEG63
- Evidence EEG64
- Evidence EEG65
- Litebox
- Neuromonitor
- Neuron-Spectrum-4/EPM
- Neuron-Spectrum-5
- Neuron-Spectrum-61
- Neuron-Spectrum-62
- Neuron-Spectrum-63
- Neuron-Spectrum-64
Showing 12 of 13 declared devices.
Catalogue references include 212001-NMD, 212002-02-NMD, 212002-NMD, 212003-NMD, 218000-NMD, 219000-02-NMD.
European nomenclature codes declared: Z12100302, Z12100401.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | Neuromedex GmbH (DE) · FDA 3009829742 |
| Devices in EUDAMED | 13 |
| Country of registration | France |
⚠️ A similar name exists; we do not assert it is the same company — why.
Device-level evidence
| Devices with a numeric GTIN | 13 |
|---|---|
| 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.