• ABBOTT BinaxNOW™ COVID-19 Antigen Self Test 2 Tests/PK

ABBOTT BinaxNOW™ COVID-19 Antigen Self Test 2 Tests/PK Covid Test - Office Ready

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    Regular price $ 24.95 Sale

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    Product Description

    IN STOCK, LIMITED SUPPLY!! 
    Due to FDA Guidelines and Supply Chain Demands All Orders for These Products are NON-Cancellable and NON-Returnable

    PLEASE NOTE: THIS PRODUCT WILL SHIP WITHIN SAME DAY if placed by 3PM PST  hours (M-F) IF YOU NEED YOUR ORDER EXPEDITED PLEASE FEEL FREE TO CONTACT US @ via chat!

    *ALL COVID ANTIGEN TESTS ARE NOT APPLICABLE TO SHIPPING OR DISCOUNT PROMOTIONS

    *This product is excluded from shipping promotion

    The BinaxNOW™ COVID-19 Antigen Self Test is a lateral flow immunoassay intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 from individuals with or without symptoms or other epidemiological reasons to suspect COVID-19 infection when tested twice over three days with at least 36 hours between tests. This test is authorized for non-prescription home use with self-collected direct anterior nasal (nares) swab samples from individuals aged 15 years or older or adult collected anterior nasal swab samples from individuals aged two years or older.

    Benefits: 

    • Detects active COVID-19 infection
    • Detects multiple strains, including the DELTA variant*
    • Results in 15 minutes
    • Easy to follow illustrated step-by-step instructions
    • Requires a minimally invasive nasal swab sample
    • Know your result now, without the need to wait for results from your healthcare provider
    • Each kit box contains two test cards to enable you to test yourself twice within 3 days, with at least 36 hours between tests
    • Compatible with the NAVICA app to capture your results for self reporting
    Test type Nasal swab Test
    Specimen type Anterior nasal (AN)
    Turnaround time 15 minutes
    Dimensions 9.125” L x 0.938” D x 5.063” H
    Each Kit contains 2 BinaxNOW™ COVID-19 Antigen Test Cards, 2 Nasal Swabs, 2 Reagent Bottles
    FDA status Emergency Use Authorization 

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