Nunex Worldwide, SA
PT-MF-000048317 · Portugal · Viana do Castelo
Nunex Worldwide, SA is registered in the European database on medical devices as a manufacturer, with 34 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 34 |
|---|
Devices declared under this manufacturer
- Intimus L Plus 40
- Intimus L Super 40
- Intimus M Maxi 15
- Intimus Maxi 60x60 10
- Intimus Maxi 90x180 15
- Intimus Plus 60x60 30
- Intimus Super 60x60 25
- Intimus Super 60x90 25
- Intimus Super 90X180 25
- Intimus Super XL 20
- Intimus XL Maxi 12
- Intimus XL Maxi 40
Showing 12 of 34 declared devices.
Catalogue references include NNX01812, NNX201244, NNX202029, NNX203026, NNX701867, NNX702956.
European nomenclature codes declared: T04010103, T04010201, T04010202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 34 |
| 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 | 34 |
|---|---|
| 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. Nunex Worldwide, SA was not found in either the U.S. or the Canadian register.