Flex2000 - Produtos Flexíveis, SA
PT-MF-000023371 · Portugal · Ovar
Flex2000 - Produtos Flexíveis, SA is registered in the European database on medical devices as a manufacturer, with 13 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 13 |
|---|
Devices declared under this manufacturer
- MEDIFLEX ANTI-ESCARAS ARTICULADO
- MEDIFLEX ANTI-ESCARAS ARTICULADO SUPRA
- MEDIFLEX HOSPITALAR I (ANTI-ESCARAS))
Showing 12 of 13 declared devices.
Catalogue references include 3-MA1002, 3-MA1003, 3-MA1020, 3-MA1207, 3-MB1002, 3-MB1004.
European nomenclature codes declared: V080702.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 13 |
| 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 | 13 |
|---|---|
| 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. Flex2000 - Produtos Flexíveis, SA was not found in either the U.S. or the Canadian register.