OCTIKA
FR-MF-000050179 · France · MAUGUIO
OCTIKA is registered in the European database on medical devices as a manufacturer, with 1 226 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 1 226 |
|---|
Devices declared under this manufacturer
- OSA258_C3
Showing 12 of 1 226 declared devices.
Catalogue references include MG027_C1, MG027_C3, OP408_C4, OP412_C1, RA_C1_200, SP4194_C4.
European nomenclature codes declared: Q02100202, Q02100201, Q0210030102, Q02100203, V030201.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 1 226 |
| 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 | 1 226 |
|---|---|
| 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. OCTIKA was not found in either the U.S. or the Canadian register.