Technix S.p.A.
IT-MF-000007797 · Italy · Grassobbio
Technix S.p.A. is registered in the European database on medical devices as a manufacturer, with 121 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 121 |
|---|
Among these devices, 121 are declared active.
Devices declared under this manufacturer
- ACCORD
- ACCORD 40
- ACCORD DR
- COMPACT DR PLUS
- EVO R+ FP
- RADIUS EVO
- REVEAL MOBI-PRO 40kW
- SYMBOL FP XL
- TCA 7
- VISITOR T30 C
- VISITOR T30 C-DR
- VISITOR T30 R
Showing 12 of 121 declared devices.
Catalogue references include 4695609000, 4695609300, 4695611900, 49.40.005.043, 49.40.005.064, ACCORD-DR/BCR.
European nomenclature codes declared: Z11039016, Z11039017, Z11039099, Z11030503.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 121 |
| 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 | 120 |
|---|---|
| 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. Technix S.p.A. was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
007/MDR | reissued | 2031-06-28 |