Laboratoire Huckert's International
BE-MF-000024078 · Belgium · Wavre
Laboratoire Huckert's International is registered in the European database on medical devices as a manufacturer, with 25 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 3 |
|---|---|
| Class IIb | 22 |
Devices declared under this manufacturer
- UMONIMU38® Labocid
- UMONIUM38 Neutralis
- UMONIUM38® Equipments 125ml
- UMONIUM38® Equipments 1L
- UMONIUM38® Equipments 5L
- UMONIUM38® Instruments 125ml
- UMONIUM38® Instruments 1L
- UMONIUM38® Instruments 5L
- UMONIUM38® Medical Spray 250ml
- UMONIUM38® Medical Tissues 1pc
- UMONIUM38® Neutralis 125ml
- UMONIUM38® Probes 100pc
Showing 12 of 25 declared devices.
Catalogue references include PF10320, PF10325, PF10520, PF10749, PF10800, PF12310.
European nomenclature codes declared: D0901.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 25 |
| 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 | 25 |
|---|---|
| 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. Laboratoire Huckert's International was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
BE26/00000024 | issued | 2031-01-28 |