MG DEVELOPPEMENT
FR-MF-000012708 · France · MAUGUIO
MG DEVELOPPEMENT is registered in the European database on medical devices as a manufacturer, with 7 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 7 |
|---|
Among these devices, 7 are declared active.
Devices declared under this manufacturer
- AUDINELL PerfectDome
- AUDIOLINE PerfectDome
- KINDeasycharger Set 2.0
- audifon charge & dry R
- neutral charge & dry R
Catalogue references include 1 HEART/B&C-138A, 1 HEART/B&C-138B, AUDF1 HEART/B&C-139A, AUDF1 HEART/B&C-139B, BAL1 PDO-59A, KIND1 HEART/B&C-140A.
European nomenclature codes declared: Y214580.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | MG DEVELOPPEMENT (FR) · FDA 3006979687 |
| Devices in EUDAMED | 7 |
| Country of registration | France |
Device-level evidence
| Devices with a numeric GTIN | 7 |
|---|---|
| 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: United States only. MG DEVELOPPEMENT is registered in the United States but was not found in the Canadian register.