Laboratoires Marie-Louise SRL
BE-MF-000001978 · Belgium · ANDERLECHT
Laboratoires Marie-Louise SRL is registered in the European database on medical devices as a manufacturer, with 9 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 9 |
|---|
Most frequent device types declared: DEP25.01/A.06, DEP25.02/A.03, XPL T9, XPL T9-2.
Devices declared under this manufacturer
- DÉPARAZ FLASH
- DÉPARAZ POUX 100ML
- DÉPARAZ POUX 200ML
- DÉPARAZ POUX PROTEX 150ML
- DÉPARAZ POUX XPULSE 150ML
- DÉPARAZ-PRO
- SHAMPOUX EXPRESS
- SHAMPOUX EXPRESS 100ML
- SHAMPOUX EXPRESS 200ML
Catalogue references include CRYSTAL FAMILY LOTION TRAITANT 200ML, CRYSTAL LOTION FLASH TRAITANT 150 ML, CRYSTAL LOTION TRAITANT 100 ML, CRYSTAL LOTION TRAITANT 100 ML (BE) FR/NL/DE, CRYSTAL SHAMPOING PRÉVENTIF 150 ML, CRYSTAL SHAMPOING TRAITANT 150 ML.
European nomenclature codes declared: V901001.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 9 |
| 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 | 9 |
|---|---|
| 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. Laboratoires Marie-Louise SRL was not found in either the U.S. or the Canadian register.