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COVID-19 TEST KITS

Clinically Validated COVID-19 rapid result blood test. Results in 10 minutes.  Intended for testing individuals showing symptoms of COVID-19.

Acute Infection Antibody Test (IgM)

1) Determines COVID-19 infection.
*Patient with positive result recommended for quarantine

Evidence of Previous Infection – Further Observation Required (IgG)
IgG Detects presence of antibodies to determine if patient has sufficiently recovered from COVID-19 Infection.

*Accuracy requirement for a test of this type is 92%

Easy to administer 10 minute rapid test – one drop of blood. 

.*Available now in bulk orders. Volume Discounts start at 100,000.

To Order Call: (877) 288-4118

This COVID-19 test detects both the IgM, acute phase antibodies which are present right before the patient becomes symptomatic and they begin tapering off at around 7 days with COV-19 and the IgG phase antibodies, which are the secondary phase antibodies whose concentrations become clinically measurable around 7 days and are generally considered to be indicative of a patient’s immune status. With COV-19, IgG antibodies will be present was exposed but regardless of whether a patient has been symptomatic or not.

This is essential for companies wanting to get a healthy workforce back to work and prevent situations where one person could infect others.

Featured COVID-19 Antibody Test Kit

Fact Sheet For Recipients – Download Here

Fact Sheet for Healthcare Providers – Download Here

This IgM/IgG dual test is a 10-minute antibody test that determines acute infection of COVID-19 virus.  Additionally, this determines if the patient has sufficiently recovered from the infection.

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Please Note:

  • 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 circumatnces 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. – 360 bbb-3(b)(1), unless the authorization is terminated or revoked sooner.

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(877) 288-4118