Alliande - Expert Manufacturer, Lda
PT-MF-000029328 · Portugal · Sintra
Alliande - Expert Manufacturer, Lda is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 8 |
|---|
Devices declared under this manufacturer
- 6BGen Máscara Cirúrgica
- Soro Fisiológico Dimor 1 L
- Soro Fisiológico Dimor 500 mL
- Soro Fisiológico Holbasic 1L
- Soro Fisiológico Wells 500 mL
- Sérum Physiologique French Pharma 1 L
Catalogue references include P2100004, P2100005, P2100006, P2100007, P2100008, P2100010.
European nomenclature codes declared: Q030103, T020604.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 8 |
| 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 | 8 |
|---|---|
| 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. Alliande - Expert Manufacturer, Lda was not found in either the U.S. or the Canadian register.