COVID-19 At-Home Rapid Self Test, Results in 15 Minutes (FDA EUA Authorized), Non-invasive Nasal Swab, Easy to Use & No Discomfort (2-PACK)

We have teamed up with manufacturers to offer FDA Authorized At-Home Rapid Self Test for the novel coronavirus, SARS-CoV-2, the virus that causes COVID-19.

Included in the Package: 2 Complete Set of COVID-19 of Antigen Rapid Tests. Each of the two single-use test kits comes with everything needed to conduct a COVID-19 test. 

• Non-Invasive At Home Test – FDA Authorized, Easy, Convenient, and Fast
• This test kit can be stored at room temperatures.
• Ships the next day. In Stock. (USPS delays may occur out of our own reach due to COVID-19, please see your local USPS announcements)
  
  

Quick in-home testing takes away the worry of developing symptoms.
Back to school, back to the office, or just back from travel or public gatherings, a rapid,15-minute, self-test is waiting at home for when you get back. The COVID-19 Antigen Rapid Test is a lateral flow assay intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2. 

• FDA Authorized 15-Minute Self-Test: Get instant COVID test results in 15 minutes! COVID-19 Antigen Rapid Test is the simplest way to detect SARS-CoV-2 nucleocapsid protein antigen. It only takes 4 steps and 15 minutes to complete the test. The test is also non-invasive. You won't need to collect a sample from deep in your nasal cavity to get accurate results.
  
  
  
  
  
  
  
  
  
• Easy to Use: Test can be done by inserting 1/2 to 3/4 inch of a simple non-invasive nasal swab. Step-by-step instructional videos are available in our app (App is optional). Its compact size makes it easy to store it away or take it with you in a travel bag. New variants have shown that anyone can be vulnerable to COVID-19 even if they are vaccinated or young. With COVID-19 Antigen Rapid Test, you can test yourself after being out in public. Early and regular testing helps you better care for yourself and protects your friends, family, and community members from potential exposure.
  
  
  
  
  
  
• COVID-19 Antigen Rapid Test app is available for iOS or Android phones: The app contains specific step-by-step video instructions to complete the test. Based on the clinical trial results, where the test was compared to an FDA-authorized molecular SARS-CoV-2 test, the test correctly identified 94.3% of positive specimens and 98.1% of negative specimens.
  
  
• Manage Group Testing Via Mobile App: The Self-Test app allows the administrator of a small group to monitor and track the group members’ test results as needed at school, work or an event.
  
  
  
  Click here for How to use the COVID-19 Antigen Rapid Test
  
  
  Legal Disclaimer
  The COVID-19 Antigen Rapid Test is a lateral flow assay intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2. This test is authorized for non-prescription home use with self-collected anterior nasal (nares) swab samples from individuals aged 15 years or older with symptoms of COVID-19 within the first seven days of symptom onset. This test is also authorized for non-prescription home use with adult-collected nasal swab samples from individuals aged 2 years or older with symptoms of COVID-19 within the first seven days of symptom onset.
  
  This test is also authorized for non-prescription home use with self-collected anterior nasal (nares) swab samples from individuals aged 15 years or older, or adult collected anterior nasal swab samples from individuals aged 2 years or older, with or without symptoms or other epidemiological reasons to suspect COVID-19 when tested twice over three days with at least 24 hours (and no more than 48 hours) between tests.
  
  This COVID-19 Antigen Home Test Kit has not been FDA cleared or approved. It has been authorized by the FDA under an Emergency Use Authorization. It has been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens, and 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. 360bbb-3(b)(1), unless the declaration is terminated, or the authorization is revoked sooner.
  
  
  

Click here for COVID-19 Test Kit FDA EUA Letter
Click here for COVID-19 Test Kit FDA EUA Letter
Click here for COVID-19 Test Kit FDA EUA Letter
Click here for COVID-19 Test Kit FDA EUA Letter
Click here for COVID-19 Test Kit FDA EUA Letter
Click here for COVID-19 Test Kit FDA EUA Letter

Q: I am having symptoms, when will my order ship?
A: We try to ship all orders on the next day.

Q: How can I get assistance for my order?
A: If you need help with your order, please e-mail us at customercare@canopusgroup.us for further assistance.

Q: Where is my order?
A: For up-to-the-minute information on the whereabouts of your order, please check the tracking information emailed to you or via the USPS website.

Q: Can I change my order for quantity/variation once the order is submitted?
A: To make a change in the quantity, please email us at customercare@canopusgroup.us to make such a request. If you want less than you already ordered, you will automatically be refunded for the removed items. In case that you need more of the already ordered products, we can make the change for you. You will be requested to make an extra payment for the added quantity and the order will be processed accordingly.

Q: Where do you ship from?
A: We are based in Orange County, California, and ship from our warehouse directly to the customer’s location.

Q: Will this test detect COVID-19 variants? 
A: Our test has completed testing on several heat inactivated variant strains and the COVID-19 Antigen Rapid Test was able to detect the mutations. 

Q: How accurate is the COVID-19 Antigen Rapid Test? 
A: Based on the results of a clinical study where the COVID-19 Antigen Rapid Test was compared to an FDA authorized molecular SARS-CoV-2 test, theCOVID-19 Antigen Rapid Test correctly identified 94.3% of positive specimens and 98.1% of negative specimens. 
Additional asymptomatic individuals and individuals beyond the seven days of symptom onset were tested, but excluded from the primary performance calculations because they were not included in the intended use. A higher proportion of low positive specimens were observed in these populations, resulting in PPAs between of 85-88% in these individuals.

Q: Does this test require an app or online account to get my results? 
A: No. Use of the app is optional. You can follow the paper instructions to perform the test if you wish. However, we do recommend you use the COVID-19 Test App as step-by-step instructional videos are available in the app for a more intuitive understanding of how to perform the test correctly. In addition, the health pass and group testing features in the app would benefit you in your daily life.

Q: How does The COVID-19 Antigen Rapid Test work?
A: The COVID-19 Antigen Rapid Test is an antigen test. When COVID-19 is present in the body, your nasal secretions can also contain the SARS-CoV-2 virus (the virus that causes COVID-19). The COVID-19 Antigen Rapid Test is able to detect small parts of the SARS-CoV-2 virus, known as N protein or antigens, in your nasal secretions.

Q: How many tests are in one box?
A: The package includes 2 complete set of COVID-19 Antigen Rapid Tests. Each of the two single-use test kits comes with everything needed to conduct a COVID-19 test.

Q: Do I always need to perform two tests?
A: No, you can use both tests whenever you want. You can use it later yourself or have your friends or relatives use it.

Q: Will this test work if I don’t have symptoms?
A: Yes. If you do not have COVID-19 symptoms, you will need to perform two tests over two or three days with at least 24 hours and no more than 48 hours between tests.

Q: Should people who have been vaccinated use this test?
A: Individuals can utilize this test, as needed, regardless of vaccination status.

Q: Is a prescription required to perform this test?
A: You do not need a doctor’s prescription to purchase and perform this test.

Q: What should I do if I have COVID-19 symptoms BUT my test result is negative?
A: If you test negative and continue to experience COVID-19 like symptoms of fever, cough, and/or shortness of breath you should seek follow-up care with your healthcare provider. Your healthcare provider may suggest you need another test to determine if you have contracted the virus causing COVID-19. If you are concerned about your COVID-19 infection status after testing or think you may need follow-up testing, please contact your healthcare provider as well.

If you will not have an additional test to determine if you are contagious, the CDC currently recommends that you should stay home until three things have happened:

• You have had no fever for at least 24 hours (that is one full day of no fever without the use of medicine that reduces fevers)

• Other symptoms of COVID-19 are improving (for example, when your cough or shortness of breath has improved) Note: Loss of taste and smell may persist for weeks or months after recovery and need not delay the end of isolation

• At least 10 days have passed since your symptoms first appeared.

Q: What does it mean if I have invalid test results?
A: Invalid result means that the test is not performed correctly. You will need to retest with a new test kit.

Q: I received an invalid result when I performed the test and I need to use a new test kit. Can I use the same sample I used in the previous test?
A: No, do not reuse any test components. Please obtain a new test kit and perform a new test.

Q: How far do I need to insert the Nasal Swab?
A: Gently insert the entire absorbent tip of the swab (usually 1/2 to 3/4 of an inch) into your nostril.

With children, the maximum depth of insertion into the nostril may be less than ¾ of an inch, and you may need to have a second person to hold the child’s head while swabbing.

Q: Is there an expiration date?
A: Yes. The COVID-19 Antigen Rapid Tests are good for 6 months after manufacture, which is compliant with what FDA has authorized to this product. You will find the printed expiration date on the back of the box.

Q: What is the shelf life of the kits after shipment?
A: Generally speaking, the COVID-19 Antigen Rapid Tests are good for 6 months after manufacture, which is compliant with what FDA has authorized to this product. Each pack of test kits has a printed expiration date on it. We will not ship any expired products to our customers.

Q: Will this test satisfy US governmental requirements for airplane travel?
A: You need to consult your airline company to see if the FDA OTC EUA approved Covid-19 antigen test result is acceptable for them. You can also find more information from the CDC website: https://www.cdc.gov/quarantine/fr-airline-faqs.html

Q: Could you use your own Q-tip to collect the sample?
A: Our swab was designed to effectively collect specimens from a person's nostrils. We can't guarantee if the Q-tip cotton swabs would perform the same way and the results can be inaccurate.

Q: Do the results indicate when the test was taken? I'll soon be required to show a negative test taken within the last 24 hours.
A: If you follow the instructions in our COVID-19 Antigen Rapid Test app to complete the test, you will receive a Health Pass in your account showing your test results along with the test date & time.

Q:How do you obtain proof of negative results that can be shown to others?
A: To show people your results, you can download the app on your phone and use the health pass. The health pass and group testing features in the app would benefit you in your daily life.

Q: The description says it tests for SARS-CoV-2. Is that the same as COVID-19?
A: Yes. COVID-19 is the name of the disease being caused by the SARS-CoV-2 coronavirus.