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NEW YORK – Qiagen said on Monday that it has obtained CE IVD marking for its NeuMoDx Flu A-B/RSV/SARS-CoV-2 Vantage Test to help healthcare professionals identify and differentiate between patients with common seasonal respiratory infections and COVID-19.

The test is now available in the European Union and other markets recognizing CE-IVD marking. Qiagen has also submitted the test to the US Food and Drug Administration for Emergency Use Authorization.

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