Oasipor - Medical, S.A.
PT-MF-000002957 · Portugal · Penafiel
Oasipor - Medical, S.A. is registered in the European database on medical devices as a manufacturer, with 284 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 284 |
|---|
Most frequent device types declared: Batas, Batas Cirúrgicas, Campos operatórios Não Estéreis, Coberturas Cirúrgicas, Coberturas mesa Não Estéreis.
Among these devices, 126 are declared sterile.
Devices declared under this manufacturer
- Bata Cirúrgica Reforçada Spunlace XXL
- Bata Cirúrgica Standard Spunlace M
- Campo Cirúrgico Autoadesivo 90x75cm
- Campo Cirúrgico Autoadesivo Reforçado 200x100cm
- Campo Cirúrgico Autoadesivo Reforçado 240x150cm
- Campo de Oftalmologia com Bolsa Dupla 160x140cm
- Cobertura Mesa Instrumentos Reforçada 190x150cm (Envoltório)
- Cobertura Mesa de Instrumentos Reforçada L, 150x190 cm
- Cobre Sapatos, TNT para Cardíaca 39x29cm
- Patient gown - tunic
- Premium scrub suit - size M
- Scrub suit pants, size XL
Showing 12 of 284 declared devices.
Catalogue references include 201114, 201114 A NE, 212115 R NE, 212126 R NE, 214141 NE, 215120.
European nomenclature codes declared: T0202, T0299, T020199, T0205, T030199, T020102.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 284 |
| 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 | 284 |
|---|---|
| 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. Oasipor - Medical, S.A. was not found in either the U.S. or the Canadian register.