DiagnostIQ Korlátolt Felelősségű Társaság
HU-MF-000046944 · Hungary · Budapest
DiagnostIQ Korlátolt Felelősségű Társaság is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- AILife Basic OKOSLELET
- AILife Normál OKOSLELET
- AILife Pajzsmirigy Basic OKOSLELET
- AILife Pajzsmirigy Extra OKOSLELET
- AILife Pajzsmirigy Prémium OKOSLELET
- AILife Prémium OKOSLELET
Catalogue references include 5999577910001, 5999577910032, 5999577910049, 5999577910063, 5999577910094, 5999577910100.
European nomenclature codes declared: W02069092.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| Country of registration | Hungary |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 6 |
|---|---|
| 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. DiagnostIQ Korlátolt Felelősségű Társaság was not found in either the U.S. or the Canadian register.