EU → North America Device Access

PAVIS SPA

IT-MF-000018588 · Italy · BUGUGGIATE

PAVIS SPA is registered in the European database on medical devices as a manufacturer, with 619 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa619

Most frequent device types declared: LINEA COLLO SPALLA, LINEA ERNIA E CONTENZIONE, LINEA ESTETICA, LINEA GAMBA GINOCCHIO, LINEA MANO BRACCIO POLSO.

Devices declared under this manufacturer

Showing 12 of 619 declared devices.

Catalogue references include 034 BL S, 131 NE SX M, 553 H33 CR M, 554 GS XXXL, 572 GS XXXL, 603BC L.

European nomenclature codes declared: Y060406, Y060308, Y061209, Y061299, Y090699, Y060312.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED619
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 GTIN619
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. PAVIS SPA was not found in either the U.S. or the Canadian register.

Other manufacturers in Italy

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