EXPERT LAB EUROPE, S.L.
ES-MF-000033270 · Spain · MADRID
EXPERT LAB EUROPE, S.L. is registered in the European database on medical devices as a manufacturer, with 23 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 23 |
|---|
Devices declared under this manufacturer
- E-SUC CLEANER
- E-SUC JET
- E-SUC PLUS
- EXPERT BENZ
- ISO LAB
- LAB 2000 PLUS
- LAB 2000 ULTRA
- ROYAL LAB 2000
- STARLINE
- ULTRA LAB
- VIDU
Showing 12 of 23 declared devices.
Catalogue references include EXP0021000, EXP0051000, EXP0055000, EXP0061000, EXP0095000, ROY0051000.
European nomenclature codes declared: D0899, D0801.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 23 |
| Country of registration | Spain |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 23 |
|---|---|
| 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. EXPERT LAB EUROPE, S.L. was not found in either the U.S. or the Canadian register.