CURA FARMA SRL
IT-MF-000011478 · Italy · MADDALONI
CURA FARMA SRL is registered in the European database on medical devices as a manufacturer, with 11 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 11 |
|---|
Most frequent device types declared: CURAMED BENDA ORLATA, CURAMED CHAMBERNEB, CURAMED CURA NEB KIT, CURAMED FISIOTAPE, CURAMED RHINONEB.
Among these devices, 1 are declared sterile.
Devices declared under this manufacturer
- CURAMED
- CURAMED CURAHOT
- CURAMED HOT&COLD
- CURAMED RHINONEB
- CURAMED UMIDIFCATORE BOTTIGLIA
- ULTRASOUND GEL 5000 ML
Catalogue references include 25310, 25369, 25531-AQUA2, 25715 - 25730, 25905, 26234.
European nomenclature codes declared: R060202, Z120610, V9099, M030101, M9001, M03030202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 11 |
| Country of registration | Italy |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 11 |
|---|---|
| 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. CURA FARMA SRL was not found in either the U.S. or the Canadian register.