EU → North America Device Access

Diapath S.p.A. società a socio unico

IT-MF-000027016 · Italy · Martinengo

Diapath S.p.A. società a socio unico is registered in the European database on medical devices as a manufacturer, with 152 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Most frequent device types declared: ALCOHOLIC COLOURLESS MIXTURE, ALCOHOLIC DEGREE 70 - DIAWHITE 70, ALCOHOLIC COLOURLESS MIXTURE, ALCOHOLIC DEGREE 95 - DIAWHITE 95, GENERAL FIXATIVE - MICROZINC - ZINC FORMALIN - READY TO USE (FORMALDEH, SINGLE-USE BOTTLE PRE-FILLED WITH BUFFERED FORMALDEHYDE FOR THE FIXATI, STAINING SOLUTION - ALCIAN BLUE pH 2.5 ACC. MOWRY.

Devices declared under this manufacturer

Showing 12 of 152 declared devices.

Catalogue references include 070190, C0053, C0223, F0096, N0165, SC041.

European nomenclature codes declared: W01030799, W01030705, W01030708, W05030501, W0202059085, W0503900201.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED152
Country of registrationItaly

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

Device-level evidence

Devices with a numeric GTIN152
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. Diapath S.p.A. società a socio unico was not found in either the U.S. or the Canadian register.

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