Previs S.r.l.
IT-MF-000017072 · Italy · Trissino (VI)
Previs S.r.l. is registered in the European database on medical devices as a manufacturer, with 55 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 55 |
|---|
Devices declared under this manufacturer
- BENDA DI GARZA IDROFILA CAMBRIC 25 FILI 5m x 100cm
- BENDA DI GARZA ORLATA 20 FILI 10m x 10cm
- BENDA DI GARZA ORLATA 20 FILI 2m x 5cm
- BENDA DI GARZA ORLATA 20 FILI 3,5m x 7cm
- BENDA DI GARZA ORLATA 20 FILI 5m x 7cm
- BENDA DI GARZA ORLATA 23 FILI 5m x 5cm
- BENDA ORLATA 20 FILI 5m x 10cm PZ 1
- BENDA ORLATA AURICOLARE 5m x 1cm
- BENDA ORLATA AURICOLARE 5m x 2cm pz 1
- Dermaplast Gazebinde 6cm x 10cm 10 Stuck
- HALLEN BENDA DI GARZA ORLATA 7cmx 3m
- PRESTERIL BENDA DI GARZA ORLATA 5cm x 5m
Showing 12 of 55 declared devices.
Catalogue references include 16280, 17F100101, 23F050051, 411150, 8007, AUR0500210PR.
European nomenclature codes declared: M030101.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 55 |
| Country of registration | Italy |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 55 |
|---|---|
| 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. Previs S.r.l. was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
0425-MDR-030043-01 | issued | 2028-10-01 |