HOW IT WORKS
Our Leadership
Meet the Maxim Biomedical Leadership Team
Our Leadership
Meet the Maxim Biomedical Leadership Team
For more information on ordering, please contact us at cleardetect@maximbio.com
COVID-19
Antigen Home Test
EASY TO USE - simple nasal swab test
FAST RESULTS - in 15 minutes
Proven to Detect Omicron & Other Variants!
COVID-19 Antigen Home Test - testing right from the privacy and comfort of your own home!
The MaximBio ClearDetect™ COVID-19 Antigen Home Test is an antigen test that allows you to detect proteins from the virus that causes COVID-19.
Made easy - An over-the-counter, no prescription needed nasal swab test you can do anywhere & anytime. Know your COVID-19 status in as little as 15 minutes!
Now Available in 2 & 25 Test Packs
The MaximBio ClearDetect™ COVID-19 Antigen Home Test is only for use under the Food and Drug Administration’s Emergency Use Authorization. It is authorized for non-prescription self-use and/or as applicable for an adult lay user testing another person 2 years or older. The test is to be used in individuals within 5 days of symptom onset or individuals without symptoms or other epidemiological reasons to suspect COVID-19 infection when tested twice over three days with at least 24 hours (and no more than 48 hours) between tests.
SIMPLE. ACCESIBLE. RAPID. SECURE.
HOW IT WORKS
1. SWAB
2. MIX
3. INSERT
4. RESULTS
Collect Nasal Swab Specimen.
Mix Swab with the Buffer in the tube.
Snap off swab handle, insert test strip, & cap tube.
Wait 15 minutes and read results visually.
Note: Before using the test, it is important to read the user instructions for more detailed instructions and additional details (included in the package).
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FREQUENTLY ASKED QUESTIONS
FOR USE UNDER FDA EMERGENCY USE AUTHORIZATION (EUA) ONLY
This product has not been FDA cleared or approved, but has been authorized by FDA under an EUA;
This product has been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens; and,
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. § 360bbb3(b)(1), unless the declaration is terminated or authorization is revoked sooner.