AUTO RIBEIRO LDA
PT-MF-000002814 · Portugal · Vila Nova de Gaia
AUTO RIBEIRO LDA is registered in the European database on medical devices as a manufacturer, with 153 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 153 |
|---|
Most frequent device types declared: CARRINHO M8, CARRINHO M860, ESTRADO E400, ESTRADO GAIA LS, MACA F3.
Devices declared under this manufacturer
- A150
- C600
- CARRINHO F3
- CARRINHO M8
- CARRINHO M860
- E250
- E400
- GAIA LS
- M760
- M764
- MACA F3
- MACA M860
Showing 12 of 153 declared devices.
Catalogue references include F001002001ACP, F002003009ACP, F002006001ACP, F002020001ACCB, F003013004APV, F005005001BPP.
European nomenclature codes declared: V08050102, V080502.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 153 |
| Country of registration | Portugal |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 153 |
|---|---|
| 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. AUTO RIBEIRO LDA was not found in either the U.S. or the Canadian register.