DIATECH SRL
IT-MF-000029128 · Italy · Milano
DIATECH SRL is registered in the European database on medical devices as a manufacturer, with 11 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 11 |
|---|
Most frequent device types declared: BARREL, EYE BATH, FLAT, FLAT ONE, FLIP BOX.
Devices declared under this manufacturer
- BARREL
- EYE BATH
- FLAT
- FLAT ONE
- FLIP BOX
- HEMA FLAT
- ICA EYE BATH
- OPTIKA FLAT
- QUALIMED FLAT
- STICK
- VIAL
Catalogue references include BARREL, FLAT, FLIP BOX, HEMA FLAT, ICA EYE BATH, OPTIKA FLAT.
European nomenclature codes declared: Q02030204, Q0299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 11 |
| 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 | 11 |
|---|---|
| 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. DIATECH SRL was not found in either the U.S. or the Canadian register.