GAZ PURS ET FLUIDES
FR-MF-000003878 · France · PLAILLY
GAZ PURS ET FLUIDES is registered in the European database on medical devices as a manufacturer, with 48 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 48 |
|---|
Most frequent device types declared: SDGM-AB, SDGM-ABCDIJKLMPQRN, SDGM-ABCEI, SDGM-ABCEIN, SDGM-ABCIN.
Among these devices, 3 are declared sterile, 48 active.
Devices declared under this manufacturer
- Système de Distribution de Gaz Médicaux
- Système de distribution de gaz médicaux
Showing 12 of 48 declared devices.
Catalogue references include SDGM-AB, SDGM-ABCDIJKLMPQRN, SDGM-ABCEIN, SDGM-ABCN, SDGM-BN, SDGM-D.
European nomenclature codes declared: A99.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 48 |
| 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 | 48 |
|---|---|
| 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. GAZ PURS ET FLUIDES was not found in either the U.S. or the Canadian register.