eMed COVID-19 Telehealth Kit, 6 Pack, 6 Tests, FDA EUA Approved COVID-19 Rapid Antigen Test for Home Use, Clinical Evaluation and Prescription

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The Men's Counter
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$48.24 - $124.24 /PC
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The Men's Counter
29 North Maple St. Duqoin IL 62832
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Don't leave:eMed's COVID-19 Telehealth kit is more than just a COVID antigen test. It's a travel essential. Deliver the telehealth access and validated lab results you need, anytime, anywhere. Scan the box and start accessing professional medical products using the real-time processor.

Get results in minutes: With eMed's COVID-19 Telehealth kit, everything you need is in the box. Each kit includes an access card for telehealth access, a COVID-19 rapid antigen test, and a validated lab report.

24/7 Home On-Demand Wireless Phone: After scanning the access card, you will be connected to a telehealth processor with step-by-step instructions (Chinese not necessarily supported). Assigned to guide you as you perform the COVID-19 rapid antigen test. Verified results are sent directly to your email, so you can enjoy peace of mind without leaving home.

Your health and safety: Our COVID-19 wireless health kit lets you screen, detect and treat common diseases from anywhere, taking care of your hands. Complemented by our easy-to-use home test kits, proven results can be anywhere you need to go in just minutes.

Results you can trust: We have the largest network of certified professional medical administrators. A community of more than 4 million consumers, businesses and government entities use our Telehealth Suite solutions to feel better and move faster.


Important information

Legal Disclaimer

This product has not been FDA cleared or approved but has been authorized by FDA under an Emergency Use Authorization (EUA). This product 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 authorization is revoked sooner.

Product Description

Rapid Care At A Click With No Clinics

Get-Together Ready in 15 Minutes!

Get-Together Ready in 15 Minutes!

Easy access to testing means easy access to the world. Test at any time, anywhere because your next adventure is just 15 minutes away with eMed.

*eMed partners with a network of licensed clinicians and pharmacists who can prescribe treatment in all 50 states

How it Works
the emed difference
2pac

HSA/FSA eligible

*eMed partners with a network of licensed clinicians and pharmacists who can prescribe treatment in all 50 states. Treatment availability is subject to a telehealth consultation with a licensed clinician, which is included with this Telehealth Kit. Not all persons may be eligible or qualify to receive a prescribed treatment. Included treatments are subject to change. Please contact your healthcare provider if you are not prescribed treatment and are still not feeling well.

Accurate Testing and Access to 24/7 On-Demand Telehealth

Proper testing and accurate results are necessary to help save lives and slow the spread of COVID-19. eMed’s telehealth proctors are available 24/7 to help ensure testing sessions are properly administered.

Our platform enables this supervision to occur remotely, protecting you and your loved ones from potential exposure.

  • Access to 24/7 On-Demand Telehealth Visits
  • FDA EUA Authorized COVID-19 Rapid Antigen Test
  • Clinical Evaluation
  • Verified Results for Travel Available in Minutes
  • Prescription included, if eligible
  • Reduced Direct Medical Costs
Fast Medication Pickup Within Hours

FDA EUA Authorized

The eMed COVID-19 Telehealth Kit includes the FlowFlex COVID-19 Ag Card Home Test, a product that has not been FDA cleared or approved but has been authorized by FDA under an EUA for use by authorized laboratories. This product has been authorized only for the detection of proteins from SARS-CoV-2, not for other viruses or pathogens. This 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. § 360bbb-3(b)(1), unless the declaration is terminated or authorization is revoked sooner.

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