Hubert De Backer nv
BE-MF-000020418 · Belgium · Temse
Hubert De Backer nv is registered in the European database on medical devices as a manufacturer, with 211 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIa | 211 |
|---|
Most frequent device types declared: Dosing applicators, Applicators, Plugs - PIBAs (Press In Bottle Adapters).
Among these devices, 188 are declared with a measuring function.
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 | Similar name found — unverified |
|---|---|
| Matched entry | HUBERT DE BACKER N.V. (BE) · FDA 3003192903 |
| Devices in EUDAMED | 211 |
| Country of registration | Belgium |
⚠️ A similar name exists in the FDA register. We do not assert that it is the same company — the two registers share no common identifier, and a name alone is not proof. This entry needs a human check.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
BE24/00000031 | issued | 2029-02-09 |