EU → North America Device Access

Pres Block S.p.A.

IT-MF-000029037 · Italy · Caselette

Pres Block S.p.A. is registered in the European database on medical devices as a manufacturer, with 4 808 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIb4 671
Class IIa137

Most frequent device types declared: ASSIEMI FLESSIBILI, UNITÀ TERMINALI AGSS ED ACCESSORI PER IMPIANTI DI EVACUAZIONE DEI GAS, UNITÀ TERMINALI PER GAS MEDICALI COMPRESSI E PER VUOTO.

Among these devices, 4 808 are declared active.

Catalogue references include IGTN-P-50-N, VEGA120/IC, VGTA-OR-A4/FM, VGTBS-OR-O/SH, VGTDM-OR-C/TD, VGTDM-OR-P/AN.

European nomenclature codes declared: Z120309.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED4 808
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 GTIN4 808
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. Pres Block S.p.A. was not found in either the U.S. or the Canadian register.

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