Laboratoires Gilbert
FR-MF-000001710 · France · Hérouville Saint-Clair
Laboratoires Gilbert is registered in the European database on medical devices as a manufacturer, with 96 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 87 |
|---|---|
| Class IIb | 8 |
| Class I | 1 |
Among these devices, 32 are declared sterile, 31 active.
Devices declared under this manufacturer
- A-CERUMEN Higiena uszu
- A-CERUMEN Hygiène des oreilles
- FLUIMAR Igiene nasale
- GILBERT Eau purifiée stérile
- HUMER DAILY NASAL HYGIENE MONODSE
- MARIMER BABY Blocked nose and cold
- MARIMER BABY Nasal hygiene
- MARIMER Blocked nose and cold
- MARIMER Hipertoniczny
- PARASIDOSE Soin traitant anti-poux et lentes
- PHYSIODOSE Hypertonique
- PHYSIODOSE Mouche bébé avec filtre
Showing 12 of 96 declared devices.
Catalogue references include 604282, 604327, 605834, 617251, 667202C, 719031.
European nomenclature codes declared: Q030103, Q0299,Q030103,V9099, Q03040299, V901001, V9099, Q030199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 96 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 43 |
|---|---|
| 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 Gilbert was not found in either the U.S. or the Canadian register.