DIA.PRO DIAGNOSTIC BIOPROBES S.R.L.
IT-MF-000029123 · Italy · SESTO SAN GIOVANNI (MILANO)
DIA.PRO DIAGNOSTIC BIOPROBES S.R.L. is registered in the European database on medical devices as a manufacturer, with 14 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: DP5, EBVDNAQT.CE, ENTERONE.CE, HSV1DNAQT.CE, JCVDNAQT.CE.
Devices declared under this manufacturer
- DIA.CHEMILUX HSV 2 IgM
- DIA500
- Dengue virus NS1 Ag
- EBV DNA Quantitation (QT)
- ENTEROVIRUS ONE-STEP
- HEV IgM
- HEV RNA QUANTITATION (QT)
- HSV1 DNA Quantitation (QT)
- JCV DNA Quantitation (QT)
- ORPHIA Chemiluminescence Immunoassay Analyzer
- Parvovirus B19 IgM
- SARA
Showing 12 of 14 declared devices.
Catalogue references include DENS1AG.CE, DP5, ENTERONE.CE, HSV1DNAQT.CE, JCVDNAQT.CE, S.A.R.A..
European nomenclature codes declared: W0201020102, W0105040611, W0105010304, W0105040311, W0204, W0105040502.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 14 |
| 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 | 14 |
|---|---|
| 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. DIA.PRO DIAGNOSTIC BIOPROBES S.R.L. was not found in either the U.S. or the Canadian register.