ROSSIELLO SRL
IT-MF-000048415 · Italy · Montemarciano
ROSSIELLO SRL is registered in the European database on medical devices as a manufacturer, with 48 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 48 |
|---|
Devices declared under this manufacturer
- CLIP LENTE BLU
- CLIP LENTE ROSSA
- DEX LENTE GIALLA
- DEX LENTE ROSSA
- EVAN LENTE ROSSA
- LENTI GREZZE BLU
- LENTI GREZZE GIALLE
- LUXURY LENTE TRASPARENTE
- PETIT CHERIE
- RAINBOW MAN
- RAINBOW MARIPOSA
- SISSI LENTE GIALLA
Showing 12 of 48 declared devices.
Catalogue references include 3344, 9131, ROS02, ROS07, ROS08, ROS13.
European nomenclature codes declared: Q0210030102, Q0210010101, Q0210030103.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 48 |
| 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 | 48 |
|---|---|
| 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. ROSSIELLO SRL was not found in either the U.S. or the Canadian register.