DEVINTEC SAGL
CH-MF-000020271 · Switzerland · Lugano
DEVINTEC SAGL is registered in the European database on medical devices as a manufacturer, with 41 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class I | 36 |
|---|---|
| Class IIa | 5 |
Authorised representative in the Union: DEVINTEC HEALTH S.L..
Devices declared under this manufacturer
- Fybocalm Wind & Bloating Relief
- GAVIDARM HÄUFIGER DURCHFALL
- GAVIDigest FLATULENCES & BALLONNEMENTS
- Gavidarm Häufige Verstopfung
- Gavidigest Constipation
- Gavidigest Diarreia
- Gavidigest Diarrhèe
- Gavidigest Diarrhée
- Gavidigest Gases e hinchazon
- Gavidigest Gases e inchaço
- Gaviscon Intestino Gonfiore e meteorismo
- Gelsectan Ibutin
Showing 12 of 41 declared devices.
Catalogue references include C05B02E008, C05B02E030, C05B02E060, C12B02E003, C12B02E03, C12B02E030.
European nomenclature codes declared: G0401, M9002, U0803.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 41 |
| Country of registration | Switzerland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 40 |
|---|---|
| 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: Neither register. DEVINTEC SAGL was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
IT336677 | issued | 2028-09-07 |
IT326645 | supplemented | 2028-09-07 |
IT325651 | supplemented | 2028-09-07 |