AQUISEL S.L.U.
ES-MF-000020750 · Spain · Abrera
AQUISEL S.L.U. is registered in the European database on medical devices as a manufacturer, with 63 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
Most frequent device types declared: AQUISEL AQUISFEK, AQUISEL Blood Collection Tubes, AQUISEL Erythrocyte Sedimentation Rate Devices.
Devices declared under this manufacturer
- AQUISFEK
- Blood Collection Tubes
- Erythrocyte Sedimentation Rate Devices (ESR)
Showing 12 of 63 declared devices.
Catalogue references include 1501028, 1501976, 1581204, 1581205, 1581974, 1780010.
European nomenclature codes declared: W050101010201, W050101010202, W02029001, W05019001.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | AQUISEL S.L. (ES) · FDA 3010352064 |
| Devices in EUDAMED | 63 |
| Country of registration | Spain |
⚠️ A similar name exists; we do not assert it is the same company — why.
Device-level evidence
| Devices with a numeric GTIN | 63 |
|---|---|
| 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.