Air Liquide Santé France
FR-MF-000001204 · France · Paris
Air Liquide Santé France is registered in the European database on medical devices as a manufacturer, with 43 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 43 |
|---|
Devices declared under this manufacturer
- Medical CO2 laparoscopy/colonoscopy B10 IT
- Medical CO2 laparoscopy/colonoscopy B11 ES/P
- Medical CO2 laparoscopy/colonoscopy B13 BE/LU
- Medical CO2 laparoscopy/colonoscopy B13 CH
- Medical CO2 laparoscopy/colonoscopy B13 DE
- Medical CO2 laparoscopy/colonoscopy B13 PI NL
- Medical CO2 laparoscopy/colonoscopy B14 IT
- Medical CO2 laparoscopy/colonoscopy B4 CH
- Medical CO2 laparoscopy/colonoscopy B40 DE
- Medical CO2 laparoscopy/colonoscopy B5 FR
- Medical CO2 laparoscopy/colonoscopy B50 FR
- Medical CO2 laparoscopy/colonoscopy B50 NL
Showing 12 of 43 declared devices.
Catalogue references include M4500C05, M5100S04R0A001, M5100S13R0A001, M5110L47R0A001, M5110L50I0A001, M5110M14R0A001.
European nomenclature codes declared: V0901, V0902.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 43 |
| 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. Air Liquide Santé France was not found in either the U.S. or the Canadian register.