BES Srl
IT-MF-000034821 · Italy · Roma
BES Srl is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 4 |
|---|---|
| Class IIa | 1 |
Most frequent device types declared: CarboBes, CarboBesFAKE, LaserBes, LaserSurgeBes, RVM Medical System.
Among these devices, 5 are declared active.
Devices declared under this manufacturer
- CarboBes
- CarboBesFAKE
- LaserBes
- LaserSurgeBes
- RVM Medical System
Catalogue references include CarboBes, CarboBesFAKE, LaserBes, LaserSurgeBes, RVM Medical System.
European nomenclature codes declared: Z12029008, Z12040201, Z12011016, Z12069099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 5 |
| 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 | 1 |
|---|---|
| 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. BES Srl was not found in either the U.S. or the Canadian register.