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Flu Test Kits in Bulk
Detect Influenza A & B in just 15 minutes. A combined test also exists to detect COVID-19 too. Tests are easy to administer, and perfect for schools, businesses, organizations, events and large gatherings.
Also offering COVID-19, RSV and Strep tests in bulk. Click here for all tests.
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We carry different Flu test kits
so there is one to fit your specific needs
LifeSign StatusTM COVID-19/Flu Test - 25 pack
Status COVID-19/Flu tests are the only FDA EUA visually read rapid test for simultaneous detection and differential diagnosis - no additional equipment needed! These tests are authorized for on-site settings operating under a CLIA certificate, and all tests that we carry have FDA Emergency Use Authorization (EUA). All tests should be administered by trained medical professionals.
- Results in 15 minutes
- 3 tests in 1 consolidates and speeds workflow
- No equipment (analyzer) needed
- COVID-19 Test - sensitivity of 93.1% and specificity of 100%
- Flu A - sensitivity of 91.4% and specificity of 95.7%
- Flu B - sensitivity of 87.6% and specificity of 95.9%
- 25 tests in each box, 25 capsules of extraction, 25 sterile swabs
- For prescription use only
- Authorized for on-site settings operating under a CLIA certificate
- Instructions for Use
- FDA EUA Letter
- Extended Shelf Life
LifeSign Status™ Flu A&B Test - 25 pack
The LifeSign Status Flu A&B Test detects influenza type A and type B antigens directly from a nasal swab. The kit includes positive and negative control swabs as well as an innovative design for the sample extraction. The LifeSign test differentiates between Influenza A and B with a pre-measured developer solution capsule for increased accuracy.
- Results in 10-15 minutes
- Differentiates between Influenza A & B
- Flu A – sensitivity of 89.2% and specificity of 99.4%
- Flu B – sensitivity of 86.4% and specificity of 99.0%
- CLIA WAIVED with nasal & nasopharyngeal swab specimens
- For prescription use only
- Instructions for Use
- Safety Data Sheet
Which Test is Right For Your Organization
| Test Kit | Use Case | Tests/Kit | Reagents/Kit | FDA | CLIA Complexity | Prescription Required | Results |
|---|---|---|---|---|---|---|---|
| LifeSign StatusTM COVID-19/Flu Test | Point-of-Care | 25 | 25 |  |
Waived | |
15 minutes |
| LifeSign StatusTM Flu A&B Test | Point-of-Care | 25 | 25 | |
Waived - Nasal & Nasopharyngeal Swabs Moderate Complexity - Nasopharyngeal Wash/Aspirate Samples | |
10-15 minutes |
Frequently Asked Questions
What happens if I receive a positive result?
If you receive a positive result you should remain in self-isolation, and inform your healthcare provider of your result. You should follow the guidance provided by the Centers for Disease Control and Prevention (CDC).
If you develop emergency warning signs for COVID-19, get medical attention immediately. Emergency warning signs include*:
If you develop emergency warning signs for COVID-19, get medical attention immediately. Emergency warning signs include*:
- Difficulty breathing or shortness of breath
- Persistent pain or pressure in the chest
- New confusion or inability to arouse
- Bluish lips or face *This list is not all inclusive. Please consult your medical provider for any other symptoms that are severe or concerning.
What does FDA authorized mean?
When there is a critical situation impacting health and safety and there are no FDA-approved or cleared tests available, and other criteria are met, the FDA can make tests available under an emergency access mechanism called an Emergency Use Authorization (EUA). The EUA for this test is supported by the Secretary of Health and Human Service’s (HHS’s) declaration that circumstances exist to justify the emergency use of in vitro diagnostics for the detection and / or diagnosis of the virus that causes COVID-19.
Select tests have been issued an Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA) for prescription home use, which provides consumers with the ability to test themselves from the comfort and safety of their homes.
Select tests have been issued an Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA) for prescription home use, which provides consumers with the ability to test themselves from the comfort and safety of their homes.
What does CLIA Waived mean?
CLIA Waived devices are the least complex. In order to receive CLIA Waived status, a manufacturer must demonstrate that a device is simple to use, has low risk to public health, and that an untrained person can get accurate results by reading the instructions.
What is the difference between Influenza A & Influenza B?
While the symptoms of influenza B mirrors those of A, the main difference between the two strains is who it can affect. Strains of influenza B are exclusively contracted by humans, while A can be carried (and spread) by animals, however, both strains are transmitted mainly by respiratory droplets from coughing and contact with an infected person. This allows strains of A to be spread more rapidly than B, while also meaning strains of B cannot cause pandemics with symptoms likely less severe. Flu shots protect against both strains of influenza.
What does Sensitivity and Specificity mean?
In a diagnostic test, Sensitivity is a measure of how well a test can identify true positives. In a diagnostic test, Specificity is a measure of how well a test can identify true negatives. Based on analysis, the sensitivity and specificity of tests, our BinaxNOW and QuickVue rapid antigen tests, are not impacted by variants.
How do I place a bulk order for my organization or institution?
For bulk order inquiries, please fill out the quote form at the top of this page with as much detail as possible pertaining to your request.
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