Reactivos para Diagnóstico
ES-MF-000022523 · Spain · Sentmenat
Reactivos para Diagnóstico is registered in the European database on medical devices as a manufacturer, with 195 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- Brain Hearth Infusion (BHI)
- Burkholderia cepacia Selective Agar (BCSA)
- Burkholderia cepacia Selective Agar Base (BCSA Base)
- CHROMagarTM Acinetobacter MDR Agar
- CHROMagarTM Candida
- CLED AGAR
- COLETSOS MEDIUM
- GBS Modified Agar
- Löwenstein-Jensen Pyruvate Medium
- MUELLER-HINTON AGAR (Modified)
- SELENITE BROTH BASE
- STUART RINGERTZ TRANSPORT MEDIUM
Showing 12 of 195 declared devices.
Catalogue references include 01-047-500, 02-598-005, 03-454-005, ALPA0076, ALPA6201, DC1736.
European nomenclature codes declared: W0104010101, W0104010206, W0104010604, W0104010402, W0104010403, W0104010404.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 195 |
| 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 | 195 |
|---|---|
| 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. Reactivos para Diagnóstico was not found in either the U.S. or the Canadian register.