bonyf AG
LI-MF-000000739 · Liechtenstein · Vaduz
bonyf AG is registered in the European database on medical devices as a manufacturer, with 15 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 15 |
|---|
Most frequent device types declared: Tablets.
No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | BONYF AG (LI) · FDA 8020152 |
| Devices in EUDAMED | 15 |
| Country of registration | Liechtenstein |
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
50537-60-00-03 | supplemented | 2027-04-18 |