EURO DIFFUSION MEDICALE
FR-MF-000001850 · France · DOMONT
EURO DIFFUSION MEDICALE is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 8 |
|---|
Most frequent device types declared: PC250/24B, PC250/24P, PC250/24SP.
Devices declared under this manufacturer
- GEL ECHOGRAPHIE POLARIS 5L
- GEL ECHOGRAPHIE POLARIS BLEU FLACON 250ML
- GEL ECHOGRAPHIE POLARIS FLACON 250ML
- GEL ECHOGRAPHIE PREMIUM CUBI 5L
- GEL ECHOGRAPHIE PREMIUM FLACON 250ML
- GEL ECHOGRAPHIE SONECHO 5L
- GEL ECHOGRAPHIE SONECHO FLACON 250ML
Catalogue references include CG5000, CG5000B, CG5000SP, PC250/24B, PC250/24P, PC250/24SP.
European nomenclature codes declared: Z11049085.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | EURO DIFFUSION MEDICALE (FR) · FDA 3013181568 |
| Devices in EUDAMED | 8 |
| Country of registration | France |
Device-level evidence
| Devices with a numeric GTIN | 8 |
|---|---|
| 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. EURO DIFFUSION MEDICALE is registered in the United States but was not found in the Canadian register.