EU → North America Device Access

Seleo S.r.l.

IT-MF-000045668 · Italy · Torre del Greco

Seleo S.r.l. is registered in the European database on medical devices as a manufacturer, with 28 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Most frequent device types declared: Adalya 40, Adalya 40 IFE, Electrophoresis automated system, Hydra 09 Plus, Microphor.

Catalogue references include PCP, SL-100-SP, SL-200-SP/2, SL-25-IFIX, SL-400-SP, SL-400-SP-HR.

European nomenclature codes declared: W01010235, W0201050101, W0103010202, W0103010504, W0102019099, W0101050101.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED28
Country of registrationItaly

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

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. Seleo S.r.l. was not found in either the U.S. or the Canadian register.

Other manufacturers in Italy

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