Amplifon S.p.A
IT-MF-000012109 · Italy · Milan
Amplifon S.p.A is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIa | 5 |
|---|
Most frequent device types declared: OtoPad.
Among these devices, 5 are declared active, 3 with a measuring function.
Devices declared under this manufacturer
- Amplifon App
Catalogue references include AMP-APP-001, APP-002, OTK001, OTP001, OTR001.
European nomenclature codes declared: Z121401, Y214599.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | AMPLIFON (IT) · FDA 9611864 |
| Devices in EUDAMED | 5 |
| Country of registration | Italy |
⚠️ A similar name exists; we do not assert it is the same company — why.
Device-level evidence
| Devices with a numeric GTIN | 5 |
|---|---|
| Found in the U.S. device database | 1 |
| Share | 20.0 % |
Canadian market access
| Health Canada licence listing | Similar name found — unverified |
|---|---|
| Matched entry | AMPLIFON SPA |
⚠️ A similar name exists; unverified — why.