NorrDia Belgium bv
BE-MF-000003701 · Belgium · Tienen
NorrDia Belgium bv is registered in the European database on medical devices as a manufacturer, with 7 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 7 |
|---|
Most frequent device types declared: HF03, HF07+, HF12, HF19, RPE00.
Among these devices, 7 are declared sterile.
Devices declared under this manufacturer
- Accusol
- Aquamax
Catalogue references include HF03, HF07+, HF12, HF19, RPE00, RPE02.
European nomenclature codes declared: F0499, F01060303, F01060103, F01060203.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 7 |
| 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 | 7 |
|---|---|
| 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. NorrDia Belgium bv was not found in either the U.S. or the Canadian register.