EU → US Device Access

AD SWISS MEDTECH SA

CH-MF-000037918 · Switzerland · Gravesano

AD SWISS MEDTECH SA is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa5

Most frequent device types declared: DP002 Vibra GO, DP006 MONOS, DP001 Vibra 3.0, DP005 PONOS, DP003 MERT.

Among these devices, 5 are declared active.

Authorised representative in the Union: IT-AR-000029315.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED5
Country of registrationSwitzerland
⚠️ Absence here is not proof of absence from the market. A manufacturer may reach the United States through a distributor registered under its own name, or under a corporate name we could not match. We publish what we measured, not what we inferred.

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