ARIA WHEELS SRL
IT-MF-000021633 · Italy · Roma
ARIA WHEELS SRL is registered in the European database on medical devices as a manufacturer, with 11 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 11 |
|---|
Most frequent device types declared: 2.0, Aero.
Devices declared under this manufacturer
- 1.0
- 2.0
- Aero
- Agile
- Buddy
- Flexy
- Halo
- KID
- PLIXA
- Speciale
- ULTRA
Catalogue references include ARIA1_0, ARIAAG, ARIAKID, ARIAPX, ARIASPE, ARIAUL.
European nomenclature codes declared: Y122106, Y180939.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 11 |
| 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 | 11 |
|---|---|
| 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. ARIA WHEELS SRL was not found in either the U.S. or the Canadian register.