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Bayer Consumer Care AG

CH-MF-000014141 · Switzerland · Basel

Bayer Consumer Care AG is registered in the European database on medical devices as a manufacturer, with 37 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class I35
Class IIa2

Most frequent device types declared: Bepanthen Itch Relief.

Authorised representative in the Union: DE-AR-000006698.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED37
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.

Notified body certificates

CertificateStatusExpiry
G70 054972 0039issued2030-03-24
G70 054972 0038issued2030-02-17

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