Artur Salgado S.A.
PT-MF-000002810 · Portugal · Vila Verde
Artur Salgado S.A. is registered in the European database on medical devices as a manufacturer, with 46 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class I | 46 |
|---|
Most frequent device types declared: Granules 0.25-0.5 (5cc vial), Granules 0.25-0.5mm (0.5cc syringe), Granules 0.5-1 mm (2cc Syringe), Granules 0.5-1.0 (vial 5cc), Granules 1-2mm (2.5cc vial).
Among these devices, 46 are declared sterile, 46 implantable.
Devices declared under this manufacturer
- AdvanCore
Showing 12 of 46 declared devices.
Catalogue references include GR0505D, GR0505V, GR1005V, GR2025V, GR6005S, GR6005V.
European nomenclature codes declared: P900401.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 46 |
| 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 | 46 |
|---|---|
| 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. Artur Salgado S.A. was not found in either the U.S. or the Canadian register.