INDIBA S.A.U.
ES-MF-000001243 · Spain · Sant Quirze del Vallès
INDIBA S.A.U. is registered in the European database on medical devices as a manufacturer, with 89 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 84 |
|---|---|
| Class IIb | 5 |
Among these devices, 13 are declared active.
Devices declared under this manufacturer
- Activ CT9
- CAPACITIVE ELECTRODE Ø23 mm
- CAPACITIVE ELECTRODE Ø50 mm
- CAPACITIVE ELECTRODE Ø60 mm
- CAPACITIVE SMART ELECTRODE Ø30 mm
- CAPACITIVE SMART ELECTRODE Ø65 mm
- Capacitive electrode 30 mm ø
- Capacitive electrode 40 mm ø
- Capacitive electrode 65 mm ø
- ELITE NS
- F2 fascia Long
- RESISTIVE SMART ELECTRODE Ø90 mm
Showing 12 of 89 declared devices.
Catalogue references include 279864MED/279864, ACC0686MED/ACC0686, ELE0129MED/ELE0129, ELE0130MED/ELE0130, ELE0135MED/ELE0135, ELE0139MED/ELE0139.
European nomenclature codes declared: X0599,Z12040203,Z120602, Z12040203,Z120602, X0599, Z120602.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 89 |
| 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 | 89 |
|---|---|
| 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. INDIBA S.A.U. was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
055/MDR | issued | 2027-10-26 |