Messer France
FR-MF-000013256 · France · Puteaux
Messer France 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 |
|---|
Among these devices, 10 are declared active.
Devices declared under this manufacturer
- Argon Medical Cryochirurgical 300 bar B50
- Argon Medical Cryochirurgical 300 bar CV12
- Argon Medical Cryochirurgical 300 bar MP4
- Argon Medicale per criochirurgia 300 bar B50
- Argon Medicinal uso en criocirugía 300 bar B50
- Argon médical chirurgical - 200 bar
- Argón medicinal uso en cirugía B05 - ES -PT
- Azote liquide Cryothérapie et cryoconservation
- CO2 Médical pour cryothérapie
- CO2 Médical pour endoscopie
- CO2 médical pour cryothérapie B50
- Hélium médical cryochirurgical 300bar B50
Showing 12 of 15 declared devices.
Catalogue references include 101100012, 101100044, 101103504, 101107219, 102623504, 103020052.
European nomenclature codes declared: V0901, V0905, V0999, K020499, V0902.
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. Messer France was not found in either the U.S. or the Canadian register.