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Do you need to COVID-19 test kits for your patients or your employees?

Early diagnosis saves lives. Order using the form below or call us today (206) 487-4770

It's a quick, easy process. Delivery within days. Test results within minutes.

 

 

 

 

 

FEATURES & BENEFITS

 

This Rapid COVID-19 Test Kit has been FDA EUA Approved since June 19th, 2020 (Click Here For Official FDA EUA Approval Letter) and facilitates timely patient treatment decisions by providing results onsite in 10 minutes. This product is a simple, time-saving procedure that contains all the necessary reagents to detect the presence of the IgM (Active COVID Infection Antibody) and the IgG (“Immunity” Antibody). This COVID-19 Rapid Test Kit is also highly sensitive and specific with an overall 98% efficacy rate.

Early Diagnosis Saves Lives. Easy to use, affordable, accurate, advanced diagnostic tests.

 

Combined Antibody Test for COVID-19 is used to qualitatively detect IgG and IgM antibodies of the novel coronavirus in human serum, plasma or whole blood in vitro.
 

    PRECISE
  • Works with whole blood, serum, & plasma
  • Tests for both IgM and IgG antibodies
  • 98% efficacy rate
    FAST
  • 10 minutes per test
  • Intuitive visual interpretation
  • No special equipment needed
  • Easy to administer the test

 

 

 

 

HOW IT WORKS

 

Four Simple Steps:

  1. Collect blood sample
     

  2. Add the blood sample to sample well
     

  3. Place 2 drops of buffer in sample well
     

  4. Read results after 10 minutes

 

 

 

 

RESULTS

 

 

 

 

 

 

TECHNOLOGY

 

 

Provides accurate COVID-19 infection diagnosis in 10 minutes.

It is widely accepted that IgM provides the first line of defense during viral infections, followed by the generation of adaptive, high affinity IgG responses for long term immunity and immunological memory.

Therefore testing of COVID-19 IgM and IgG antibodies is an effective method for the rapid diagnosis of COVID-19 infection.

 

Furthermore, detection of COVID-19 IgM antibodies tends to indicate a recent exposure to COVID-19, whereas detection of COVID-19 IgG antibodies indicates a later stage of infection.

 

Thus, this combined antibody test could also provide information on the stage of infection.

 

 

 

 

PRODUCT INFO, TESTING DATA & FACT SHEETS

FOR MEDICAL PERSONS

 

 Review EUA Letter Download Test Data Download Clinical Report Download Recepient Fact Sheet

 

IgG and IgM Antibody (Serology) Test Kits


The FDA has authorized this test under the Emergency Use Authorization Act. The factory that produces these tests state a 98% efficacy rate. These results have been submitted and are on file with the FDA. They are also accessible on this site for your review.
 

Our quality control personnel in China reviewed and/or visited 30+ factories before we selected this test. We have tests on the ground and can accommodate orders up to 10,000,000 million pieces+.


How does the test work?


A quick finger prick for a drop of blood on the test strip will tell you if you have an active infection OR if you have had Covid-19 in the past year. The test detects both current and past antibodies in the blood that were triggered by the COVID-19 virus. This test does not determine if you are actively shedding (contagious). A positive result should be considered “active” until considered clear and virus free by a medical professional.


Noteworthy for all tests of this type from the FDA


This test has not been reviewed by the FDA. (Currently in testing for validation)
 

Negative results do not preclude acute SARS-CoV-2 infection. If acute infection is suspected, direct testing for SARS-CoV-2 is necessary. (If your Test is positive you must seek a test from a medical professional)
 

Results from antibody testing should not be used to diagnose or exclude acute SARS-CoV-2 infection. (No Covid test is 100% accurate)
 

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. (The test detects past and present infections and/or exposure)

Is it registered with the FDA?


Yes, this test is registered with the FDA and cleared for use and distribution only. Test results have been reviewed but, not approved by the FDA (a multi year process). This EUA will be effective until terminated under Section 564(b)(2) or (g) of the Act.


Who is the client for this product?

 

This a commercial product designed for use by clinical laboratories. By purchasing you agree to have this test administered by the appropriate persons.

 

How long before you get results?


The results are apparent in 10 to 15 minutes.


What if I show IgM or IgG on the test?


You should quarantine immediately and seek guidance from a medical healthcare provider. You will also need to take a PCR (polymerase chain reaction) test from a medical laboratory.


PCR vs IgG/Igm?


The PCR test looks for active pieces of the virus in the nose, throat, and respiratory airways. Covid is new and there are many viewpoints out there. Current review of numerous testing of PCR and Serology testing suggests that 5 days after initial exposure efficacy rates are similar. However, this varies wildly based on each individual person and “group results” in a lab do not equate to personal results.


What if I was exposed yesterday to COVID?


All tests become more accurate as viral load increases. Our test is not as reliable within the first 4 days of exposure. At 5 days as noted above this equally as accurate, and Beyond 8 days of contact the test should be more accurate according to a comparison of FDA test results. The average efficacy rate is 98% according to FDA approved results.

Is the test safe?


Yes, every finger prick is done with a quick release disposable needle.


Will it tell me if I have had COVID-19 before?


Yes, antibodies can sometimes stick around for 2+ years. Immunoglobulin M (IgM) is the first antibody that is formed against a germ. This antibody will appear first on test, usually within 1-2 weeks. The body then forms immunoglobulin G (IgG), which appears on test about 2 weeks after the illness starts. IgM usually disappears from the blood within a few months, but IgG can last for years.


Will it tell me if I am active?


Yes, if you come up positive for IgM then you are most likely still carrying the active COVID-19 virus in your blood. If you are positive for IgG then, you have probably had COVID-19 over two weeks ago. Remember anyone experiencing symptoms, should get a PCR (polymerase chain reaction) nasal swab test to determine if the virus is still active.

 

Will it tell me if I am I have any other viruses or pathogens?


No, Only SARS-CoV-2 IgM and IgG antibodies

 


Where else are these tests being used?


Germany uses and exports these tests around the region. These tests are also being used in China, Taiwan, Korea, Europe, the Middle East and of course now with FDA approval USA, Canada, and Mexico.


Why did you choose this factory?


The factory was chosen for its professionalism, reputation, and for the quality of its facility.

 

 

 

PRICING & SECURE PAYMENT FORM

 

Print 1-Page Price List

 

 How many units makes sense?


Businesses and healthcare facilities are increasingly being required to test their employees and patients as often as once a week (please see below articles, also check your latest local regulations)


So, for every 10 people to test, we recommend a general formula as follows: (10 people) x (4 tests/month) x (secure a 3 to 6 month supply) = 120 units to secure a 3 month supply, or 240 units for securing 6 months.

 

  

 

 

 

 

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