EU → North America Device Access

LABORATOIRES EUROMEDIS

FR-MF-000036597 · France · NEUILLY-SOUS-CLERMONT

LABORATOIRES EUROMEDIS is registered in the European database on medical devices as a manufacturer, with 248 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa248

Most frequent device types declared: CHAMPS DE SOINS ET DE TABLE STERILES, Compresses de gaze stérile, Compresses non tissées non stériles, Compresses non tissées stériles, Gant d'examen Nitrile Non poudré FLEXISKIN® 240 mm.

Among these devices, 172 are declared sterile.

Devices declared under this manufacturer

Showing 12 of 248 declared devices.

Catalogue references include 127596, 135265Z, 164005, 164112, 164300, 175435.

European nomenclature codes declared: M0201020101, T0202, M0202010101, T01020204, T020401, T02010101.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED248
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 GTIN248
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. LABORATOIRES EUROMEDIS was not found in either the U.S. or the Canadian register.

Notified body certificates

CertificateStatusExpiry
40277supplemented2030-08-05

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