EU → North America Device Access

Air Liquide Medical Systems S.A.

FR-MF-000003649 · France · Antony

Air Liquide Medical Systems S.A. is registered in the European database on medical devices as a manufacturer, with 52 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIb39
Class IIa13

Most frequent device types declared: KA010100, KA010300, KB040010, KF008003, KY692800.

Among these devices, 39 are declared active, 16 with a measuring function.

Devices declared under this manufacturer

Showing 12 of 52 declared devices.

Catalogue references include AC104300, AF301039, BM000300, CK062538, CK062539, CK062544.

European nomenclature codes declared: Z120309, Z1203010504, Z1203019080.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED52
Country of registrationFrance

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

Device-level evidence

Devices with a numeric GTIN52
Found in the U.S. device database0
Share0.0 %

Canadian market access

Health Canada licence listingSimilar name found — unverified
Matched entryAIR LIQUIDE MEDICAL SYSTEMS

⚠️ A similar name exists; unverified — why.

What it holds in Canada

Licences on record2
Currently active0
Class 3 devices2
First licensed2016-09-15

Licence types: System (2).

Licensed under: MONNAL T60, MONNAL T60 ADVANCED.

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