Industrial Médica Alicantina
ES-MF-000003913 · Spain · Elche (Alicante)
Industrial Médica Alicantina is registered in the European database on medical devices as a manufacturer, with 78 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 78 |
|---|
Among these devices, 78 are declared reusable.
Catalogue references include 10.01.12, 10.01.19, 10.02.16, 20.01.05.01, SRF01007, SRF01034.
European nomenclature codes declared: L091001.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 78 |
| 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 | 78 |
|---|---|
| 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. Industrial Médica Alicantina was not found in either the U.S. or the Canadian register.