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InBIOS

InBios Receives FDA EUA for
Smart Detect™ SARS-CoV-2 rRT-PCR Kit

In response to the COVID-19 outbreak, InBios is working diligently to develop new tests. Today, we are pleased to announced that InBios has received Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA) for our
Smart Detect™ SARS-CoV-2 rRT-PCR Kit.

This real-time PCR test is intended for the qualitative detection of nucleic acid from SARS-CoV-2, the virus that causes COVID-19.
Our test can be used in all hospital and lab systems.

    Kit tests 45 unknown patient specimens
    Sample types: human nasopharyngeal, anterior & mid-turbinate nasal swab specimens
    Results in ~4 hours
    Validated on Applied Biosystems 7500 Fast Dx Real-Time PCR and the Biorad CFX96 Touch Real-Time PCR Detection System instruments

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