MEDICAIR FACTORY SRL
IT-MF-000010184 · Italy · LIMENA
MEDICAIR FACTORY SRL is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 6 |
|---|
Most frequent device types declared: SISTEMA ANTIDECUBITO ECO PLUS AUTOACTIVE, SISTEMA ANTIDECUBITO FLOW BASE.
Among these devices, 6 are declared active.
Devices declared under this manufacturer
- EPA
- ESA
- FLOW BASE
- FLOW HIGH
- FLOW MIDDLE
- UP AIR
Catalogue references include EPA/6/00, ESA/8/00, SFLBAPU, SFLHIPU, SFLMIPU, UAI/4/00.
European nomenclature codes declared: V080701.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| 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 | 6 |
|---|---|
| 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. MEDICAIR FACTORY SRL was not found in either the U.S. or the Canadian register.