DIATECH PHARMACOGENETICS SRL
IT-MF-000018670 · Italy · JESI
DIATECH PHARMACOGENETICS SRL is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- EasyPGX ready ESR1
- EasyPGX ready HPV
- EasyPGX ready JAK2
- EasyPGX ready MGMT
- EasyPGX ready MLH1
- EasyPGX ready NPM1 Quant
- EasyPGX ready NPM1 Screening
- Myriapod NGS PGx Sign panel
Catalogue references include NGX037, RTX034, RTX047, RTX048, RTX049, RTX051.
European nomenclature codes declared: W01060299, W0106010499, W0105041003.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 8 |
| 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 | 8 |
|---|---|
| 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 PHARMACOGENETICS SRL was not found in either the U.S. or the Canadian register.