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Eurogenetics

Country not established

Devices
1

What Eurogenetics makes

Eurogenetics manufactures the EUROGENETICS CRP ELISA, a diagnostic test for detecting C-reactive protein (CRP) levels in blood samples using enzyme-linked immunosorbent assay (ELISA) technology.

The company’s portfolio is regulated under FDA’s Class II device classification and is listed in the 510(k) clearance registry. The manufacturer operates from the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Eurogenetics Crp Elisa Ref K872539

    Class II
    Active 510(k) 510(k) II

Frequently asked questions

How many devices does Eurogenetics have in the registry?

The registry currently lists 1 device for Eurogenetics. Devices recorded under merged duplicate company entries are counted once.

Which registries list Eurogenetics's devices?

Among its 1 most recently registered device, Eurogenetics has devices listed in FDA 510(k) (1 device).

What risk classes do Eurogenetics's devices fall under?

Among its 1 most recently registered device, the classes recorded for Eurogenetics's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Eurogenetics in the registry?

The most recently registered devices listed for Eurogenetics include EUROGENETICS CRP ELISA.

Generated automatically from registry data and not verified by a human reviewer.