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    Copia de PCR Mercedes Retes Labq 3

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    Maria Speroni Corbella
    This 3 sentence summary provides the key information from the medical report: The SARS-CoV2 test result for patient Maria Mercedes Retes was negative, indicating an absence of active COVID-19 infection based on the nasal sample collected. While a negative result makes active infection less likely, it does not rule out potential infection or co-infection with other viruses. The test used real time RT-PCR methodology and was authorized for emergency use by the FDA to detect nucleic acid from SARS-CoV-2.

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    Copia de PCR Mercedes Retes Labq 3

    Uploaded by

    Maria Speroni Corbella
    29 views1 page
    This 3 sentence summary provides the key information from the medical report: The SARS-CoV2 test result for patient Maria Mercedes Retes was negative, indicating an absence of active COVID-19 infection based on the nasal sample collected. While a negative result makes active infection less likely, it does not rule out potential infection or co-infection with other viruses. The test used real time RT-PCR methodology and was authorized for emergency use by the FDA to detect nucleic acid from SARS-CoV-2.

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    Copia de Pcr Mercedes Retes Labq 3

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    This 3 sentence summary provides the key information from the medical report: The SARS-CoV2 test result for patient Maria Mercedes Retes was negative, indicating an absence of active COVID-19 infection based on the nasal sample collected. While a negative result makes active infection less likely, it does not rule out potential infection or co-infection with other viruses. The test used real time RT-PCR methodology and was authorized for emergency use by the FDA to detect nucleic acid from SARS-CoV-2.

    Copyright:

    © All Rights Reserved
    Download as PDF, TXT or read online from Scribd
    Download as pdf or txt
    29 views1 page

    Copia de PCR Mercedes Retes Labq 3

    Uploaded by

    Maria Speroni Corbella
    This 3 sentence summary provides the key information from the medical report: The SARS-CoV2 test result for patient Maria Mercedes Retes was negative, indicating an absence of active COVID-19 infection based on the nasal sample collected. While a negative result makes active infection less likely, it does not rule out potential infection or co-infection with other viruses. The test used real time RT-PCR methodology and was authorized for emergency use by the FDA to detect nucleic acid from SARS-CoV-2.

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    You are on page 1of 1

    FINAL

    Martin J. King, Ph.D.


    Laboratory Director
    140 58 ST BLDNG A UNT 3L, BROOKLYN, NY 11220-2539 CLIA ID# 33D1020120
    Phys: LABQ MOBILE WASHINGTON SQUARE 4234 Patient: RETES MUNDO, MARIA MERCEDES
    55 Washington Square DOB. 10/19/1971 Room# Age:50 Sex:F
    , Phone: +1 (954) 614-9039
    ( ) - Chart#: 857615 Route#: 0
    MARTIN KING PH.D Passport: E1305269478 Page:1 of 1

    Acc# 2111191353 Coll. Date: 02/03/22 Recv. Date: 02/03/22 Final Report Date: 02/04/22
    Order# G-B224C73D Coll. Time: 04:04 PM Recv. Time: 08:15 PM Final Report Time: 02:29 AM

    Test Name Result Out of Range Normal Range Units

    Report Status: FINAL

    **********
    SARS-COV2 NEGATIVE NEGATIVE

    Source: Nasal

    This test has been authorized as an EUA for use by authorized


    laboratories. Negative results do not preclude infection of the upper
    respiratory tract. Test Methodology: RT-PCR

    - -

    This SARS-CoV-2 assay is a real time RT-PCR test for the detection of
    nucleic acid from individuals suspected of having COVID-19 infection.
    POSITIVE: Results are indicative of active infection with SARS-CoV-2 but do
    not rule out bacteria infection or co-infection with other viruses.
    NEGATIVE: Results do not preclude SARS-CoV-2 infection and should not be
    used as the sole basis for patient management decisions. If COVID-19 is
    still suspected based on clinical findings, history and epidemiological
    information, re-testing of a new specimen should be considered.
    Note: Pooling was used to generate this result. Individual specimens with
    low viral loads may not be detected due to the decreased sensitivity or
    increased interference when tested with pooled testing.
    The United States(U.S.)FDA has made this test available under an
    Emergency Use Authorization(EUA). The EUA is supported by the Secretary of
    Health and Human Services (HHS’s)declaration that circumstances exist to
    justify the emergency use of in vitro diagnostics (IVDs) for the detection
    and/or diagnosis of SARS-CoV-2. This assay has been validated pursuant to
    the CLIA regulations and may be used for diagnostic testing purposes.

    ________________________________ END OF REPORT __________________________

    L = Low; H = High; CL = Critical Low; CH = Critical High

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