ALS Life Sciences Portugal, S.A.
PT-MF-000034751 · Portugal · Tondela
ALS Life Sciences Portugal, S.A. is registered in the European database on medical devices as a manufacturer, with 18 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- InviMag® Blood DNA Mini Kit/ IG
- InviMag® Universal Kit/ KF96
- InviSorb® Spin Blood Mini Kit (250)
- InviSorb® Spin Blood Mini Kit (50)
- InviSorb® Spin Universal Kit (250)
- InviSorb® Spin Universal Kit (50)
- InviTrap® Spin Universal RNA Mini Kit (250)
- InviTrap® Spin Universal RNA Mini Kit (50)
- PSP® SalivaGene DNA Kit (250)
- PSP® SalivaGene DNA Kit (50)
- RTP® Pathogen Kit (250)
- RTP® Pathogen Kit (50)
Showing 12 of 18 declared devices.
Catalogue references include 1035200300, 1035211200, 1035231100, 1050100200, 1060100200, 1060100300.
European nomenclature codes declared: W0105900101, W05019002.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 18 |
| 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 | 18 |
|---|---|
| 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. ALS Life Sciences Portugal, S.A. was not found in either the U.S. or the Canadian register.