BIODISIN S.R.L
IT-MF-000031661 · Italy · TREVISO
BIODISIN S.R.L is registered in the European database on medical devices as a manufacturer, with 17 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 17 |
|---|
Most frequent device types declared: MIKROAIR.
Among these devices, 1 are declared active.
Devices declared under this manufacturer
- Alcawash
- BioWipes
- Closept
- MikroAir™
- MkActive™
- NeatZym
- NeatZym PLUS
- Neatzym
- Neudry
- Neutracix
- PoliWipes
- Prolub
Showing 12 of 17 declared devices.
Catalogue references include 103, 109.1, 115, 116, 118, 125.
European nomenclature codes declared: D0801, Z12011385, D0899, D99, V9099, Z12011301.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 17 |
| 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 | 17 |
|---|---|
| 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. BIODISIN S.R.L was not found in either the U.S. or the Canadian register.