EU → US Device Access

Serrix B.V

NL-MF-000005882 · Netherlands · Amsterdam

Serrix B.V is registered in the European database on medical devices as a manufacturer, with 36 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa36

No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED36
Country of registrationNetherlands
⚠️ 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
BE23/00000172supplemented2028-06-19

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