LIEVENS-LANCKMAN BV
BE-MF-000001979 · Belgium · Grimbergen
LIEVENS-LANCKMAN BV is registered in the European database on medical devices as a manufacturer, with 14 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 14 |
|---|
Most frequent device types declared: Bolus.
Devices declared under this manufacturer
- Bolus Gel, 10X10X0,5CM
- Bolus Gel, 15x20x0,5cm
- Bolus Gel, 15x20x1cm
- Bolus Gel, 30x30x0,5cm
- Bolus Gel, 30x30x1,0cm
- Bolus Gel, 30x30x1cm
- Bonnets réfrigérants / Cooling caps
- Brassards réfrigérants / Cooling wraps
- Brassards réfrigérants 15X60 cm / Cooling wraps 15X60 cm
- Chaussons réfrigérants / Cooling slippers
- Gants réfrigérants / Cooling gloves
Showing 12 of 14 declared devices.
Catalogue references include BL-9605, BL-9605 - 10 pces, BL-9905, BL-9905 - 5 pces, BL-9910, BL-9910 - 3 pces.
European nomenclature codes declared: T030499, T0306.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 14 |
| 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 | 14 |
|---|---|
| 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. LIEVENS-LANCKMAN BV was not found in either the U.S. or the Canadian register.