HIDROFER SA
PT-MF-000002824 · Portugal · CARREIRA-VILA NOVA DE FAMALICÃO
HIDROFER SA is registered in the European database on medical devices as a manufacturer, with 66 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 66 |
|---|
Most frequent device types declared: 467-001, Zaragatoa 100% Algodão.
Devices declared under this manufacturer
- Algodão Hidrófilo
- BOLAS BRANCAS DE ALGODAO HIDROFILO
- COMPRESSAS CONTINENTE 5X5
- COMPRESSAS TECIDO NÃO TECIDO
- Coton Hydrohile Pliage Accordéon 100Gr
- Cotton Hydrofhile 100 g
- ENROLADO DE ALGODAO HIDROFILO
- ROLOS DE ALGODAO HIDROFILO
- Rolo dentário BV
- Rolos Dentários de Algodão
- ZIG-ZAG ALGODÃO HIDROFILO
- ZIG-ZAG DE ALGODAO HIDROFILO
Showing 12 of 66 declared devices.
Catalogue references include 201-5x5 TNT Continente, 401-050 MILUX, 401-070 Hasse, 401-100 DON COTON, 401-100 KAIGERT, 401-100 Vitadomia.
European nomenclature codes declared: M010101, M0202010102.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 66 |
| 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 | 65 |
|---|---|
| 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. HIDROFER SA was not found in either the U.S. or the Canadian register.