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AR Baltic Medical UAB

LT-MF-000004402 · Lithuania · Vilnius

AR Baltic Medical UAB is registered in the European database on medical devices as a manufacturer, with 793 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class I684
Class IIa109

Most frequent device types declared: ELUTAX “3”-OTW 30600, ELUTAX “3”-OTW-K 100350, ELUTAX “3”-OTW-L 20300, ELUTAX “3”-OTW-L 80350, N-ELUTAX “3” 25250.

Among these devices, 793 are declared sterile.

Devices declared under this manufacturer

Showing 12 of 793 declared devices.

Catalogue references include ELUTAX “3”-OTW 30600, ELUTAX “3”-OTW-L 20300, N-ELUTAX “3” 25250, N-ELUTAX “3”-L 10225, N-ELUTAX “3”-L 13400, N-ELUTAX “3”-L 15325.

European nomenclature codes declared: C010402020101, C010401020101.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED793
Country of registrationLithuania

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

Device-level evidence

Devices with a numeric GTIN793
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. AR Baltic Medical UAB was not found in either the U.S. or the Canadian register.

Other manufacturers in Lithuania

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