SERB SA
BE-MF-000017045 · Belgium · Brussels
SERB SA is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class I | 6 |
|---|
Most frequent device types declared: 61B1001_Z3 / FP00000173, 61B1001_Z7 / FP00000176, 61B2001_Z7 / FP00000177, 61B2001_Z3 / FP00000174, 61B0501_Z3 / FP00000172.
Among these devices, 6 are declared sterile, 5 implantable.
No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| Country of registration | Belgium |
⚠️ Absence here is not proof of absence from the market. A manufacturer may reach the United States through a distributor registered under its own name, or under a corporate name we could not match. We publish what we measured, not what we inferred.