FUTURLAB S.R.L.
IT-MF-000046539 · Italy · LIMENA
FUTURLAB S.R.L. is registered in the European database on medical devices as a manufacturer, with 49 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: FCC201-2, FCC204-2, FCC206-2, FCC207-2, FCC214-2.
Devices declared under this manufacturer
- ACIDI BILIARI TOTALI LR
- ACIDO URICO LR
- ALBUMINA LR
- COLESTEROLO DIRETTO LDL
- CONTROLLO P
- CREATININA JAFFE' LR
- ENZYMATIC CREATININE LR
- EXTRA WASH
- FRUTTOSAMINA LR
- LDH LR
- LIPASI DGGR LR
- MULTICALIBRATORE
Showing 12 of 49 declared devices.
Catalogue references include FCC201-2, FCC206-2, FCC207-2, FCC219-2, FCC40-2-2, FCC50-2-2.
European nomenclature codes declared: W01019001, W0101050101, W01010207, W01010235, W01010203, W01010202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 49 |
| 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 | 12 |
|---|---|
| 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. FUTURLAB S.R.L. was not found in either the U.S. or the Canadian register.