EYE TECH CARE
FR-MF-000036680 · France · Rillieux-la-Pape
EYE TECH CARE is registered in the European database on medical devices as a manufacturer, with 9 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 9 |
|---|
Most frequent device types declared: Control unit, Probe.
Among these devices, 6 are declared sterile, 9 active.
Devices declared under this manufacturer
- EYEOP-PACK
- EyeOP1
- UCP Star control unit
- UCP Star probe
Catalogue references include ETC0200_06, ETC0911_08, ETC0912_08, ETC0913_08, ETC5111, ETC5112.
European nomenclature codes declared: Q0299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 9 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 9 |
|---|---|
| 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. EYE TECH CARE was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
40169 | supplemented | 2030-02-20 |