BAARS ET ASSOCIES
FR-MF-000025734 · France · Oyonnax
BAARS ET ASSOCIES is registered in the European database on medical devices as a manufacturer, with 154 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 154 |
|---|
Most frequent device types declared: Adventure, Alfa X, Charlie N, Charlie R, Consolidated.
Devices declared under this manufacturer
- Adventure C31 Iron Blue
- Alfa X C44 Earth Brown
- Axon - C37 Moss Green
- Charlie N C43 Coyote Brown
- Charlie R C26 Carbon Grey
- Consolidated C30 Dune Beige
- Copenhagen 2 C17 Cobalt
- Curtiss C25 Army Green
- Delta R C36 Drisftwood
- Delta X C31 Iron Blue
- Detroiter C27 Fur
- Haiku - C34 Terracotta
Showing 12 of 154 declared devices.
Catalogue references include ADV-C31, CN - C43, CON - C30, COP2 - C17, CR - C26, DR - C36.
European nomenclature codes declared: Q02100202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 154 |
| 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 |
|---|---|
| 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. BAARS ET ASSOCIES was not found in either the U.S. or the Canadian register.