GIBAUD
FR-MF-000014279 · France · SAINT-ETIENNE
GIBAUD is registered in the European database on medical devices as a manufacturer, with 1 976 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 1 976 |
|---|
Devices declared under this manufacturer
- CHUT MARESCA BLEU OCEAN T38
- CHUT SERIFOS BLEU T38
- CORFOU noir femme T35
- EGINE noir T39
- GIBAUD CHUT OLBIA Taupe T42
- LIPSI noir T40
- MADRID BLEU T40
- MADRID BLEU T45
- MALLEOGIB 3D CAVIGLIERA LEGAMENTI TG4
- MANUGIB 3D D T4D
- MANUGIB De Quervain T1D
- MANUGIB rhizarthrose immo T2D
Showing 12 of 1 976 declared devices.
Catalogue references include 6399-1, 6700-4D, 8201-35, 8237-38, 8409-38, 8425-42.
European nomenclature codes declared: Y063303, Y060308, Y061209, Y060312, Y060613, Y060612.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 1 976 |
| 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 | 1 976 |
|---|---|
| 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. GIBAUD was not found in either the U.S. or the Canadian register.