GILAC
FR-MF-000029695 · France · Marcy L'Étoile
GILAC is registered in the European database on medical devices as a manufacturer, with 15 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 15 |
|---|
Devices declared under this manufacturer
- Bassin de lit 2.5L Cooper
- Bassin de lit 2.5L blanc
- Bassin de lit anti bactérien
- Bassin de lit avec couvercle 2.5L
- Bassin de lit rond + couvercle
- Bocal à urines 2L
- Couvercle Anti bactérien
- Couvercle bassin de lit Cooper
- Couvercle bassin de lit blanc
- Crachoir
- Inhalateur 0.6L Blanc
- Urinal Homme avec couvercle
Showing 12 of 15 declared devices.
Catalogue references include G101190, G101208, G101321, G101390, G101421, G102121.
European nomenclature codes declared: V0812, R030199, V0899, V0812,W05010203.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 15 |
| 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 | 15 |
|---|---|
| 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. GILAC was not found in either the U.S. or the Canadian register.