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CASCINATION AG

CH-MF-000009927 · Switzerland · Bern

CASCINATION AG is registered in the European database on medical devices as a manufacturer, with 17 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa13
Class IIb4

Among these devices, 10 are declared active, 8 with a measuring function.

Authorised representative in the Union: DE-AR-000008247.

United States market access

FDA establishment registerRegistered with FDA
Matched entryCASCINATION (CH) · FDA 3011797532
Devices in EUDAMED17
Country of registrationSwitzerland

Notified body certificates

CertificateStatusExpiry
G10 095657 0006issued2027-05-29

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