DURVIZ, S.L.
ES-MF-000004181 · Spain · VALENCIA
DURVIZ, S.L. is registered in the European database on medical devices as a manufacturer, with 53 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: REAL SAMPLE COLLECTION KIT, SISTEMA DE RECOGIDA PARA DETECCIÓN DE ENTEROBIUS VERMICULARIS, SISTEMA DE RECOGIDA, TRANSPORTE Y CONCENTRACION DE PARASITOS EN HECES, SISTEMA DE TRANSPORTE, CONSERVACIÓN Y CONCENTRACION DE PARÁSITOS.
Devices declared under this manufacturer
- EASY PICK MINI SYSTEM/ PIPETTE 0.9ML
- REAL GRAHAM TEST
- REAL MIDI SYSTEM TOTAL FIX
- REAL MIDI SYSTEM TOTALFIX
- REAL MINI SYSTEM SIN FILTRO
- REAL MINI SYSTEM SIN MEDIO CON PERLAS
- REAL MINI SYSTEM TOTAL FIX
- REAL SALIVA DNA SAMPLE COLLECTION KIT
- REAL SWAB SAMPLE COLLECTION KIT
- REAL UNIVERSAL SYSTEM SAF
- REAL UNIVERSAL SYSTEM TOTAL FIX
- SEDIMENTATION CONE MINI SYSTEM
Showing 12 of 53 declared devices.
Catalogue references include RBMSAL01CE, RP9015, RPP03, RPP1713B, RPP2002, RPP9000BC.
European nomenclature codes declared: W0104050199, W05019002, W05019001.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 53 |
| 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 | 53 |
|---|---|
| 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. DURVIZ, S.L. was not found in either the U.S. or the Canadian register.