EU → North America Device Access

NEUT

FR-MF-000009582 · France · SAINT ANDRE LES VERGERS

NEUT is registered in the European database on medical devices as a manufacturer, with 3 043 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa3 043

Most frequent device types declared: ABIGAIL-ROSE, BALLADIN-XXL-NOIR, BLANCHE-ROSE, COLINE-NOIR, ECHARPE-IMMOBILISATION-BRAS.

Devices declared under this manufacturer

Showing 12 of 3 043 declared devices.

Catalogue references include 2401503, 490019343, 4963513538, 4975240646, 4978110545, 4993255536.

European nomenclature codes declared: Y063303, Y061203, T0299, Y061215, Y061280, M030501.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED3 043
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 GTIN3 043
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. NEUT was not found in either the U.S. or the Canadian register.

Other manufacturers in France

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