EU → North America Device Access

Idmed

FR-MF-000002402 · France · Marseille

Idmed is registered in the European database on medical devices as a manufacturer, with 60 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa60

Most frequent device types declared: ALG-System, CG-MU, CG-PS, TF2-PS, TOF-Sensor.

Among these devices, 60 are declared active, 10 with a measuring function.

Devices declared under this manufacturer

Showing 12 of 60 declared devices.

Catalogue references include ALG, CD-MU, PWR5-2_EU, PWR5-2_TI, PWR5-U_EU, PWR5-U_UK.

European nomenclature codes declared: Z1203019001, Z1203019099, Z12040101, Z12040180.

United States market access

FDA establishment registerRegistered with FDA
Matched entryIDMED (FR) · FDA 3012072872
Devices in EUDAMED60
Country of registrationFrance

Device-level evidence

Devices with a numeric GTIN60
Found in the U.S. device database37
Share61.7 %

Canadian market access

Health Canada licence listingLicensed in Canada
Matched entryIDMED

What it holds in Canada

Licences on record5
Currently active0
Class 2 devices5
First licensed2016-06-23

Licence types: System (5).

Licensed under: TOFSCAN, NEUROLIGHT, ALGISCAN, WITOF, TRACHEAL TUBE CUFF CONTROLLER.

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

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