Stiloptic di Celer Patrycja Ewa
IT-MF-000027197 · Italy · Baveno
Stiloptic di Celer Patrycja Ewa is registered in the European database on medical devices as a manufacturer, with 195 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 195 |
|---|
Devices declared under this manufacturer
- SI5011.133
- SI5021.277
- SI5022.307
- SI5033.340
- SI5039.304
- SI5556.280
- SI5557.175
- SI5565.141
- SI5566.338
- SI5566.342
- SI5567.338
- SI6515.600
Showing 12 of 195 declared devices.
Catalogue references include SI5011.133, SI5022.307, SI5039.304, SI5556.280, SI5557.175, SI5565.141.
European nomenclature codes declared: Q02100202, Q02100203, Q02100201.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 195 |
| 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 | 195 |
|---|---|
| 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. Stiloptic di Celer Patrycja Ewa was not found in either the U.S. or the Canadian register.