EU → North America Device Access

Air Liquide Italia Gas e Servizi S.r.l.

IT-MF-000007596 · Italy · Milano

Air Liquide Italia Gas e Servizi S.r.l. is registered in the European database on medical devices as a manufacturer, with 51 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa28
Class IIb23

Most frequent device types declared: AZOTO LIQUIDO D.M. DERMATOLOGIA, AZOTO LIQUIDO D.M.CRIOCONSERVAZIONE, CO2 D.M. COLTURA CELLULARE, CO2 D.M. LAPARO/COLONSCOPIA, MISCELA SPIROMETRICA D.M. MIX 1.

Among these devices, 2 are declared active, 1 with a measuring function.

Devices declared under this manufacturer

Showing 12 of 51 declared devices.

Catalogue references include FT13IDGMA80000, FT14SDEGAA0000, FT31IMPO2AMB0B, IMPIANTO DI DISTRIBUZIONE VUOTO, M4766S10R5A001, M5110M14R0A001.

European nomenclature codes declared: Z120309, Z12150185, M9001, Z12029085, V9099, Z120102.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED51
Country of registrationItaly

⚠️ Not found is not the same as not sold — how this comparison can be wrong.

Device-level evidence

Devices with a numeric GTIN50
Found in the U.S. device database0
Share0.0 %

Canadian market access

Health Canada licence listingNot found in the Canadian register

⚠️ Canada lists no Class I devices at all — what that excludes.

North American profile: Neither register. Air Liquide Italia Gas e Servizi S.r.l. was not found in either the U.S. or the Canadian register.

Other manufacturers in Italy

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