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Abbott BinaxNOW At Home Antigen Self Test in Kuwait

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Abbott BinaxNOW At Home Antigen Self Test in Kuwait
Abbott BinaxNOW At Home Antigen Self Test in Kuwait
Price And Quantity
  • Box/Boxes
  • 1
  • Box/Boxes
  • 1.2-1.5 USD ($)
  • 1.20 - 1.50 USD ($)
Product Description

Simple and Efficient: This COVID-19 Antigen Rapid Test was made by   to quickly detect Sars-CoV-2 nucleocapsid protein antigen in a person,  Abbott BinaxNOW At Home Antigen Self Test in Kuwait following only 4 simple steps of testing. Using the included highly-absorbent nasal swab, the specimen can be obtained by brushing 5 times against the inner wall of both nostrils of a patient. You can effectively get a sample just by inserting 1/2 to 3/4-inch of the swab inside the nose, since this test kit promotes optimal comfort for the user.

The specimen is then mixed with the solution inside the tube, thoroughly mixing 15 times to make sure that all the samples collected are incorporated with the buffer solution. Simply put 3 drops of the solution in the sample well of the kits COVID-19 test card, and wait for 15 minutes. Fast and precise results can help individuals and healthcare professionals be aware of the situation, which can greatly help in proper diagnosis and action.

Quick & Accurate Result: Results will automatically appear on the stick after a few minutes, and you can determine its meaning based on the result reference guide in the kit. A solo horizontal mark on the "C" (control) area depicts that you have a negative result. A positive result shows two marks for the "C" and "T" (test) zones.Abbott BinaxNOW At Home Antigen Self Test in Kuwait  Invalid results show no lines on the stick or incomplete lines.

FDA Disclaimer: This swab test kit is not FDA cleared or approved, but only authorized under an Emergency Use Authorization for home use or point of care use. It is authorized for the rapid detection of proteins from SARS-CoV-2 and not for any other viruses or pathogens. The emergency use of this product 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 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 declaration is terminated or authorization is revoked sooner.

Trade Information
  • USA
  • 3 Per Day
  • 5-15 Days
  • Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa
  • FDA EUA CE ISO GMP SFC ETC. Abbott BinaxNOW At Home Antigen Self Test in Kuwait
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Contact Us

28955, Avenue Sherman Valencia, California, Missouri, 91355, United States
Phone :+12093486395