EU → North America Device Access

Cair LGL

FR-MF-000007921 · France · Lissieu

Cair LGL is registered in the European database on medical devices as a manufacturer, with 1 921 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa1 919
Class IIb2

Most frequent device types declared: Class I - Non-sterile devices allowing administration to patient, Class I - Non-sterile devices allowing removing from patient, Class IIa - Sterile devices for infusion, Class IIa - Sterile devices for nutrition, Class IIb - Disinfectant for hydraulic circuit of hemodialysis machine.

Among these devices, 1 866 are declared sterile, 4 with a measuring function.

Devices declared under this manufacturer

Showing 12 of 1 921 declared devices.

Catalogue references include NCE06PU, NCE206G, NCE516AU-0, PES3307R-0, PO3390-0, RP5000-0.

European nomenclature codes declared: A03020101, A0702, A0703, A03040199, A0399, G02020101.

United States market access

FDA establishment registerRegistered with FDA
Matched entryCAIR LGL (FR) · FDA 3008448733
Devices in EUDAMED1 921
Country of registrationFrance

Device-level evidence

Devices with a numeric GTIN1 921
Found in the U.S. device database3
Share0.2 %

Canadian market access

Health Canada licence listingLicensed in Canada
Matched entryCAIR L.G.L.

North American profile: Both markets. Cair LGL is registered in both the United States and Canada.

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