WiQo S.p.A.
IT-MF-000028707 · Italy · Milano
WiQo S.p.A. is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 5 |
|---|
Most frequent device types declared: MG19510903, MG20111206, MG20200518.
Devices declared under this manufacturer
- FYOX
- PRX-T INTIMATE
- PRX-T Lady
- PRX-T33
Catalogue references include PFFYX001, PFMDR001, PFMDR002, PFPRL001, PFPRX020.
European nomenclature codes declared: V9099, Q01010399.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 5 |
| 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 | 5 |
|---|---|
| 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. WiQo S.p.A. was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
ECM25MDR002 | issued | 2030-02-04 |