eurocolumbus s.r.l.
IT-MF-000016861 · Italy · Milano
eurocolumbus s.r.l. is registered in the European database on medical devices as a manufacturer, with 26 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 26 |
|---|
Most frequent device types declared: Euroampli Alien Cardio, alien.
Among these devices, 26 are declared active.
Devices declared under this manufacturer
- Euroampli Alien Cardio
- alien X 3D recharge
- alien X recharge
- alien e - Vers. alien 2020
- alien e - Vers. alien 2020 cardio
- alien e - Vers. alien 2121
- alien e - Vers. alien 2121 cardio
- alien e - Vers. alien 212175
- alien e - Vers. alien 3030
- alien e - Vers. alien 303075
- alien e recharge - Vers. alien 2020 cardio
- alien e recharge - Vers. alien 2121 cardio
Showing 12 of 26 declared devices.
Catalogue references include Euroampli Alien Cardio - Vers. 2121, alien X 3D recharge, alien e recharge � Vers. alien 2020 cardio, alien e recharge � Vers. alien 3030 cardio, alien e � Vers. alien 2020, alien e � Vers. alien 2121.
European nomenclature codes declared: Z11030101,Z11039017.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 26 |
| 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 | 26 |
|---|---|
| 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. eurocolumbus s.r.l. was not found in either the U.S. or the Canadian register.