Visia imaging SRL
IT-MF-000015628 · Italy · San Giovanni Valdarno
Visia imaging SRL is registered in the European database on medical devices as a manufacturer, with 13 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIa | 13 |
|---|
Most frequent device types declared: ALADDIN HW3.0, CC-100 HW6.0 / CC-100XP HW6.0, HENSON 9000, MYAH; MYOPIA EXPERT 700, SOLOS; SOLOS Lite.
Among these devices, 11 are declared active.
Devices declared under this manufacturer
- ALADDIN HW3.0
- CA-800
- CC-100 HW6.0
- CC-100XP HW6.0
- HENSON 9000
- MYAH
- MYOPIA EXPERT 700
- SOLOS
- SOLOS Lite
- TERA Dry Eye Imager
Showing 12 of 13 declared devices.
Catalogue references include 1240212, 42-0001417, 42-0002770, 42-0002866, 42-0002941, BMT1IV.
European nomenclature codes declared: Z12120123, Z12120199, Z12120102, Z1212012003, Z12129099.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | VISIA imaging S.r.l. (IT) · FDA 3007913988 |
| Devices in EUDAMED | 13 |
| 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 | 13 |
|---|---|
| Found in the U.S. device database | 6 |
| Share | 46.2 % |
Canadian market access
| Health Canada licence listing | Similar name found — unverified |
|---|---|
| Matched entry | VISIA IMAGING S.R.L. |
⚠️ A similar name exists; unverified — why.
What it holds in Canada
| Licences on record | 6 |
|---|---|
| Currently active | 0 |
| Class 2 devices | 6 |
| First licensed | 2015-04-07 |
Licence types: Single Device (5), System (1).
Licensed under: ALADDIN HW3.0, CA-800 CORNEAL ANALYZER, MYAH, MYOPIA EXPERT 700, HENSON 9000, TERA DRY EYE IMAGER.