EU → North America Device Access

MEDIFLY S.R.L.

IT-MF-000023448 · Italy · MEDOLLA

MEDIFLY S.R.L. is registered in the European database on medical devices as a manufacturer, with 23 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa23

Most frequent device types declared: F010072, F010255, F010889, F011015, F011160.

Among these devices, 14 are declared sterile.

Devices declared under this manufacturer

Showing 12 of 23 declared devices.

Catalogue references include F010072, F010889, F011160, F01200690CN, F01300690, F017101015BU.

European nomenclature codes declared: A060102, A06010103, A0601010201, A060301.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED23
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. MEDIFLY S.R.L. was not found in either the U.S. or the Canadian register.

Other manufacturers in Italy

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