ZUITLAB, LDA.
PT-MF-000045541 · Portugal · Braga
ZUITLAB, LDA. is registered in the European database on medical devices as a manufacturer, with 7 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 7 |
|---|
Devices declared under this manufacturer
- ZUIT®
Catalogue references include ZUITEP250, ZUITEP500, ZUITHD60, ZUITHDK60, ZUITHO30, ZUITPP250.
European nomenclature codes declared: Q0199, V9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 7 |
| 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 | 7 |
|---|---|
| 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. ZUITLAB, LDA. was not found in either the U.S. or the Canadian register.