ATOL GROUP
FR-MF-000037164 · France · BEAUNE
ATOL GROUP is registered in the European database on medical devices as a manufacturer, with 53 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 53 |
|---|
Devices declared under this manufacturer
- ONEO
Showing 12 of 53 declared devices.
Catalogue references include OFT802M M M P Orange mat et acier, OFT804L M L P Bleu intense et bleu océan, OFU803M M M P Bleu intense mat et cuivre, OFU803M M M P Transparent Cristal, OFU804L M L P Brun Brillant, OFU804L M L P Noir et Argent.
European nomenclature codes declared: Q02100202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 53 |
| 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 | 53 |
|---|---|
| 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. ATOL GROUP was not found in either the U.S. or the Canadian register.