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Wondfo COVID-19 Rapid Result Test-Lateral Flow Method-20 Test/Box

SKU
MPSRM-W195
In stock
More Information
Brand Redmoby Brand
MPN W195
Packaging 20 Test/Box
$442.84

    Note : Image shown for reference purposes only. Actual product appearance may vary. Please read product description for full and accurate details

    • Rapid testing - results in 15 minutes
    • Highly accurate #1 serology test now in Europe and China
    • Simple read similar to a pregnancy test
    • Comes with everything to test 20 patients
    Product Details
    MD-W195
    W195
    Wondfo
    Usually ships in 1 day
    Ground
    Specifications
    20 test cassettes w/Wondfo imprint individually packed in pouch+20 disposable droppers+1 detection buffer (6 mL)+1 Instructions For Use (IFU)
    Two steps to perform the whole test
    86.43%
    12 months
    99.57%
    Store in room temperature (35.6-86 degrees F). If the test kit (include cassette and testing buffer) is refrigerated, resume it to the room temperature for at least 30 minutes before testing.
    Fingertip blood, venous whole blood, serum and plasma
    10 ?L
    Features
    Lancet and alcohol pad are not provided
    Rapid results in 15 minutes
    Highly accurate #1 serology test now in Europe and China
    Simple read similar to a pregnancy test
    FOR PROEFSSIONAL USE ONLY. Must attend a "How to Use" call before order will ship
    This test has not been reviewed by the FDA, but are compliant with FDA Policy for Diagnostic Test for Corona Virus Disease
    Negative results do not rule out SARS-CoV-2 infection, particularly in those who have been in contact with the virus. Follow-up testing with a molecular diagnostic should be considered to rule out infection in these individuals
    Results from antibody testing should not be used as the sole basis to diagnose or exclude SARS-CoV-2 infection or to inform infection status
    Positive results may be due to past or present infection with non-SARS-CoV-2 coronavirus strains, such as coronavirus HKU1, NL63, OC43, or 229E.
    The 1st Officially Approved Test in China
    DO NOT read the result after 20 minutes
    Successfully passed the validation based on the ?Policy for Diagnostic Tests for Coronavirus Disease- 2019 during the Public Health Emergency? issued by FDA on March 16, 2020, and has been officially listed in FDA,
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