Bruno Barbato medicali srl
IT-MF-000039449 · Italy · Napoli
Bruno Barbato medicali srl is registered in the European database on medical devices as a manufacturer, with 124 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 124 |
|---|
Most frequent device types declared: ABSORBE, FLOPPER, PROTEGO.
Among these devices, 3 are declared sterile.
Devices declared under this manufacturer
- ABSORBE
- IGO
- TAVOP
- TAVOP LAP
- TETRA
Showing 12 of 124 declared devices.
Catalogue references include 10003ELC, 10003ETK03, 1000T02, BB6090T, KRK4560, PRO10003ELC.
European nomenclature codes declared: T030501, T04010299, T0399, Q019003, T0205.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 124 |
| 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 | 124 |
|---|---|
| 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. Bruno Barbato medicali srl was not found in either the U.S. or the Canadian register.