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: 61B0501_Z3 / FP00000172, 61B0501_Z7 / FP00000175, 61B1001_Z3 / FP00000173, 61B1001_Z7 / FP00000176, 61B2001_Z3 / FP00000174.
Among these devices, 6 are declared sterile, 5 implantable.
Devices declared under this manufacturer
- COLLATAMP G
Catalogue references include 61B0501_Z3, 61B0501_Z7 / FP00000175, 61B1001_Z3 / FP00000173, 61B1001_Z7 / FP00000176, 61B2001_Z3 / FP00000174, 61B2001_Z7 / FP00000177.
European nomenclature codes declared: M040502.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| Country of registration | Belgium |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 6 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | SERB SA |
What it holds in Canada
| Licences on record | 1 |
|---|---|
| Currently active | 0 |
| Class 4 devices | 1 |
| First licensed | 2007-08-01 |
Licence types: Device Family (1).
Licensed under: COLLATAMP G.
North American profile: Canada only. SERB SA holds a Canadian licence but was not found in the U.S. register.