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: Applicators, Dosing applicators, Plugs - PIBAs (Press In Bottle Adapters).
Among these devices, 188 are declared with a measuring function.
Devices declared under this manufacturer
- Cup
- Eye shield
Showing 12 of 211 declared devices.
Catalogue references include DIA APPL CONTRA, V000325, V000580, V000929, V009046, V009263.
European nomenclature codes declared: A020299, A0280, V0402, Q0299.
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; we do not assert it is the same company — why.
Device-level evidence
| Devices with a numeric GTIN | 211 |
|---|---|
| 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.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
BE24/00000031 | issued | 2029-02-09 |