COVID-19 Ag CARD
PROCEDURE CARD
For Use Under an Emergency Use Authorization (EUA) Only.
The BinaxNOW COVID-19 Ag Card is a lateral flow immunoassay for the qualitative detection of the nucleocapsid protein antigen to SARS-CoV-2 directly from nasal swab specimens collected from individuals who are suspected of COVID-19 by their healthcare provider within seven days of the onset of symptoms.
IMPORTANT: See Product Insert, including QC section, for complete use instructions, warnings, precautions and limitations. False negative results may occur if specimens are tested past 1 hour of collection. Specimens should be tested as quickly as possible after specimen collection. Open the test card just prior to use, lay it flat, and perform assay as follows.
Part 1 – Sample Test Procedure
Patient Samples require 6 drops of Extraction Reagent.
1.Hold Extraction Reagentbottle vertically. Hovering 1/2inch above the TOP HOLE,slowly add 6 DROPS to theTOP HOLE of the swab well.DO NOT touch the cardwith the dropper tip whiledispensing.
2.Insert sample or control swabinto BOTTOM HOLE andfirmly push upwards so thatthe swab tip is visible in theTOP HOLE
3.Rotate (twirl) swab shaft3 times CLOCKWISE (tothe right). Do not removeswab.
4.Peel off adhesive liner from the right edge of the test card. Close and securely seal the card. Read result in the window 15 minutes after closing the card.In order to ensure proper test performance, it is important to read the result promptly at 15 minutes, and not before. Results should not be read after 30 minutes.
Part 2 – Result Interpretation
Negative Result
A negative specimen will give a single pink/purple colored Control Line in the top half of the window, indicating a negative result. This Control Line means that the detection part of the test was done correctly, but no COVID-19 antigen was detected. Negative results, from patients with symptom onset beyond seven days, should be treated as presumptive and confirmation with a molecular assay, if necessary, for patient management, may be performed.
Positive Result
A positive specimen will give two pink/purple colored lines. This means that COVID-19 antigen was detected. Specimens with low levels of antigen may give a faint Sample Line. Any visible pink/purple colored line is positive.
Invalid Result
If no lines are seen, or if just the Sample Line is seen, the assay is invalid. Invalid tests should be repeated.
Procedure for External Quality Control Testing
External Controls require 8 drops of Extraction Reagent
- Hold Extraction Reagent bottle vertically. Hovering 1/2 inch above the TOP HOLE, slowly add 8 DROPS to the TOP HOLE of the swab well. DO NOT touch the card with the dropper tip while dispensing.
- Follow Steps 2 – 4 of the Test Procedure shown.
In the USA, this test has not been FDA cleared or approved; this test has been authorized by FDA under an EUA for use by authorized laboratories; use by laboratories certified under the CLIA, 42 U.S.C. §263a, that meet requirements to perform moderate, high or waived complexity tests. This test is authorized for use at the Point of Care (POC), i.e., in patient care settings operating under a CLIA Certificate of Waiver, Certificate of Compliance, orCertificate of Accreditation. This test has been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens. In the USA, – this test is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of the virus that causes COVID-19 under Section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. § 360bbb-3(b)(1), unless the authorization is terminated or revoked sooner.
Technical Support Advice Line
Further information can be obtained from your distributor, or by contacting Technical Support on: US +1 800 257 9525 [email protected]
Abbott Diagnostics Scarborough, Inc.
10 Southgate Road Scarborough, Maine 04074 USA
IN195001
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