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.
Devices declared under this manufacturer
- AphtoFix
- BUCOMED CREMA FIJADORA 15g
- BUCOMED CREMA FIJADORA 70g
- BUCOMED TABLETAS LIMPIADORAS
- Denthoral
- Denture Relining Cushion Stabilizer
- Dr Max
- Express effervescent cleanser tablets for dentures and removable denta
- FARMODENT ORAL CARE SOLUTIONS COMPRESSE EFFERVESCENTI
- OlivaFix® Denture Adhesive cream
- OlivaFix® Gold denture adhesive cream 75g
- PerioCream Periodontal Paste
Showing 12 of 15 declared devices.
Catalogue references include 20.900.00.9.0.0.00, 223881.7, 32.250.00.N.0.0.01, 44.900.09.T.0.0.39, 5.940.07.18.0.0.03, 5.970.00.T.0.0.00.
European nomenclature codes declared: D99, Q010280, Q019007, Q010503, Q010304, Q010699.
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 |
Device-level evidence
| Devices with a numeric GTIN | 15 |
|---|---|
| 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. bonyf AG is registered in the United States but was not found in the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
50537-60-00-03 | supplemented | 2027-04-18 |