FUMAGALLI CARE & REHA SRL
IT-MF-000027186 · Italy · ARCORE
FUMAGALLI CARE & REHA SRL is registered in the European database on medical devices as a manufacturer, with 34 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 34 |
|---|
Most frequent device types declared: ARIEL, MITICO, OIBO', REMY, ROBIN.
Devices declared under this manufacturer
- ARIEL L
- DORY
- Mitico Expert L
- Passeggino Ypsi
- ROBIN Configurazione base mis. 2
- ROBIN Configurazione completa mis. 2
- Robin configurazione completa mis. 1
- Shifu Air mis. 1
- Shifu Air mis. 2
- Shifu Air mis. 3
- Shifu Earth mis. 3
- Shifu Ocean mis. 3
Showing 12 of 34 declared devices.
Catalogue references include 690002, 800002, 841301, 841302, 841303, 872301.
European nomenclature codes declared: Y050202, Y122703, Y180918, Y050201, Y093399, Y180999.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 34 |
| 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 | 34 |
|---|---|
| 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. FUMAGALLI CARE & REHA SRL was not found in either the U.S. or the Canadian register.