Nippon Sanso Portugal
PT-MF-000004891 · Portugal · Maia
Nippon Sanso Portugal is registered in the European database on medical devices as a manufacturer, with 39 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 39 |
|---|
Most frequent device types declared: GNIP2.
Devices declared under this manufacturer
- Nitrógeno líquido Producto Sanitario (PS) para criopreservación (GNIP2
- Nitrógeno líquido Producto Sanitario (PS) para crioterapia y criocirug
Showing 12 of 39 declared devices.
Catalogue references include LE-LD20, LE-LD50, PGS180, PGS196, PGS239, PGS45XL.
European nomenclature codes declared: V0902.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 39 |
| 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 | 39 |
|---|---|
| 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. Nippon Sanso Portugal was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
HZ 1714363-1 | amended | 2031-01-29 |
2025 CR 0059 | issued | 2030-08-11 |