MOBERCAS SL
ES-MF-000025078 · Spain · ALMAZORA
MOBERCAS SL is registered in the European database on medical devices as a manufacturer, with 215 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 215 |
|---|
Most frequent device types declared: CE-0137, CE-2150-ARPC, CE-2339-ARPC, CH-0127-R, CH-0150-ABR.
Among these devices, 202 are declared active.
Devices declared under this manufacturer
- CE-0137
- CE-2150-ARPC
- CE-2339-AR
- CE-2339-ARPC
- CE-BOBATH-0215-R
- CH-0127-R
- CH-0150-ABR
- CH-2120-BR
- CH-2130-ARPC
- CH-2140-ABR
- CH-MB20-A
- CH-MB30
Showing 12 of 215 declared devices.
Catalogue references include CE-2150-ARPC, CE-2339-ARPC, CH-0127-R, CH-0150-ABR, CH-2120-BR, CH-2140-ABR.
European nomenclature codes declared: V08050101, V08020101, Y180918, Z12130201, V080202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 215 |
| 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 | 215 |
|---|---|
| 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. MOBERCAS SL was not found in either the U.S. or the Canadian register.