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Medimaps Group SA

CH-MF-000039146 · Switzerland · Plan-les-Ouates

Medimaps Group SA is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa5

Most frequent device types declared: Software Accessory for medical image communication, Software for analysis of bone microarchitecture, V3.

Among these devices, 4 are declared active.

Authorised representative in the Union: Med-Imaps SASU.

Devices declared under this manufacturer

Catalogue references include CORELAB, OS-PTM, OS-TBSi, REVTBSRV10.

European nomenclature codes declared: Z11900192, Z11900182.

United States market access

FDA establishment registerRegistered with FDA
Matched entryMedimaps Group SA (CH) · FDA 3010208539
Devices in EUDAMED5
Country of registrationSwitzerland

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: United States only. Medimaps Group SA is registered in the United States but was not found in the Canadian register.

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