EU → North America Device Access

EUROPODEX S.L.

ES-MF-000042401 · Spain · GIJON

EUROPODEX S.L. is registered in the European database on medical devices as a manufacturer, with 32 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa32

Most frequent device types declared: Collar Cymam anátomico blando :T/S,T/M,T/L,T/XL, E1070A,EE1072A,E1070,E1072,E1090, E2100,E2101,E2102,E2103,E2104,E2105, E2135,E2146,E2140S,EE2140M,E2140L,E2145, E4100,E4200,E4300,E4400,E4500,E4600,E4700,E4800.

Devices declared under this manufacturer

Showing 12 of 32 declared devices.

Catalogue references include E2103, E2140S, E2146, E2730, E3030L, E3030S.

European nomenclature codes declared: M030501, Y122406, Y12030601, Y061209, Y060312, Y060609.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED32
Country of registrationSpain

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

Device-level evidence

Devices with a numeric GTIN32
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. EUROPODEX S.L. was not found in either the U.S. or the Canadian register.

Other manufacturers in Spain

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