COVID-19 RAPID TEST KITS

COVID-19 IgG/IgM antibody test is an FDA EUA authorized test kit, that can detect the IgG and IgM antibodies in 10 minutes with 95% accuracy.

COVID-19 RAPID TEST KITS

COVID-19 IgG/IgM antibody test is an FDA EUA authorized test kit, that can detect the IgG and IgM antibodies in 10 minutes with 95% accuracy.

Our COVID-19 Antibody Test Kits


Our COVID-19 antibody test kits are the most effective rapid results test on the market.

Rapid Test Kits:

  • Are FDA EUA authorized
  • Provide rapid results in 10 minutes
  • Have a 24-month shelf life
  • Proven high sensitivity for current infection of the virus
  • Require a verification of use case prior to shipping is mandatoryr

PLEASE NOTE THIS IS NOT FOR INDIVIDUAL PURCHASE.
THIS IS STRICTLY FOR BUSINESSES, EDUCATION
AND GOVERNMENTAL ORGANIZATIONS.

If you are an individual looking to be tested please contact your
employers Human Resources Department.

PLEASE NOTE THIS IS NOT FOR INDIVIDUAL PURCHASE.
THIS IS STRICTLY FOR BUSINESSES, EDUCATION
AND GOVERNMENTAL ORGANIZATIONS.

If you are an individual looking to be tested please contact your
employers Human Resources Department.

Brand Global your Testing Partner

We’re not just selling COVID-19 antibody test kits, we’re partnering with organizations to ensure they have the best results with their COVID-19 Rapid Testing Program.
 

If you order more than 5,000 kits, we will utilize our expertise in the healthcare industry to help map out the logistics for testing and how to safely coordinate positive tests.

We can even provide medical teams to administer tests for your company.

Deploying a Rapid Testing Program you can lower your healthcare costs, increase productivity, help recruitment, reduce “sick” days, and increase retention.

Additional Notices

  • This test has not been FDA cleared or approved;

  • This test has been authorized by FDA under an EUA for use by authorized laboratories;

  • This test has been authorized only for the presence of IgM and IgG antibodies against SARS-CoV-2, not for any other viruses or pathogens; and

  • 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 COVID-19 under Section 564(b)(1) of the Act, 21 U.S.C. § 360bbb-3(b)(1), unless the authorization is terminated or revoked sooner.

    Warning

  • This test has been authorized by FDA under an EUA for use by authorized laboratories.

  • This test has not been FDA cleared or approved.

  • This test has been authorized only for the presence of IgM and IgG antibodies against SARS-CoV-2, not for any other viruses or pathogens.

  • 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 COVID-19 under Section 564(b)(1) of the Act, 21 U.S.C. § 360bbb-3(b)(1), unless the authorization is terminated or revoked sooner.

  • 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.

  • This product is intended for professional use and not for home use.

  • Not for the screening of donated blood.