Visia Lab S.r.l.
IT-MF-000013016 · Italy · San Giovanni Valdarno (AR)
Visia Lab S.r.l. is registered in the European database on medical devices as a manufacturer, with 17 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
Most frequent device types declared: 300450051500, L-20, L-IFA, NAVILIVE, ZENIT FLOW COMPACT.
Devices declared under this manufacturer
- LOGIBIOTECH
- Logibiotech
- dIFine P30
Showing 12 of 17 declared devices.
Catalogue references include 300026_00, 300038_00, 300450051500, 49218, FA01C, FA01NC.
European nomenclature codes declared: W02060199, W02079099, W0202050303, W0201020192, W02079082, W02079092.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | VISIA LAB SRL (IT) · FDA 3026753391 |
| Devices in EUDAMED | 17 |
| Country of registration | Italy |
⚠️ A similar name exists; we do not assert it is the same company — why.
Device-level evidence
| Devices with a numeric GTIN | 17 |
|---|---|
| Found in the U.S. device database | 7 |
| Share | 41.2 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | VISIA LAB S.R.L. |
What it holds in Canada
| Licences on record | 5 |
|---|---|
| Currently active | 0 |
| Class 2 devices | 5 |
| First licensed | 2025-03-06 |
Licence types: Single Device (4), Device Family (1).
Licensed under: DIFINE ANA HEP-2 CLASSIFIER, DIFINE DNA CLASSIFIER, DIFINE IFA SLIDE PROCESSORS, DIFINE AUTOMATED MICROSCOPE, DIFINE ANCA CLASSIFIER.