SARS-CoV-2 Antigen Rapid Test

Providing an aid in early diagnosis of individuals who are suspected of COVID-19 by their healthcare provider and who are asymptomatic.

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Special Statement of Flowflex Product Versions
Date:2022-01-28 Click:

ACON Flowflex COVID-19 Antigen Home Test has received Emergency UseAuthorization (“EUA”) from the United States Food and Drug Administration(“FDA”). This makes Flowflex brandhas both a CE marked product and a FDA EUA authorized product for lay personuse.

Please be advised that the products are notinterchangeable, they comply with different regulation requirements. These twoproducts have different commercial names, different REF numbers, differentclaims, different instructions for use, and are in visually different packagingas blow.

The FlowflexSARS-CoV-2 Antigen Rapid Test, which is CE marked, is not authorized forexport to or sale in the United States market. Likewise, Flowflex COVID-19 Antigen Home Test, which is US FDA EUA cleared,is not authorized for export to or sale in the markets out of the UnitedStates. Otherwise, the products will be confiscated and destroyed by theSupervisory Authority, leading to a loss for the seller as well as thepotential for further legal action, due to mislabeled (including unauthorized),defective, or otherwise fraudulent products.

If you are aware of any non-compliant sales activities, please contact us:

Telephone: +86-571-8777-5555