SpeedySwab™ Rapid COVID-19 + Flu A&B Test

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SpeedySwab^™ Rapid COVID-19 + Flu A&B Test

4.9

| TRUSTED BY 50,000+

$395.00

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A groundbreaking solution for the simultaneous detection of COVID-19, Influenza A, and Influenza B in just 15 minutes.

25 tests per box
Detects: COVID-19 (SARS-CoV-2), Influenza A, and Influenza B.
FDA Emergency Use Authorization (EUA) approved.

Size: Single

Single

3 Boxes

5 Boxes

10 Boxes

Free Shipping over $250. Get it shipped today.

Pro-Tip

Pair your SpeedySwab™ Rapid COVID-19 + Flu A&B Test with CofixRX™ Anti-Pathogen (Povidone Iodine) Nasal Cleanse for an extra layer of protection. CofixRX is formulated with povidone-iodine to help reduce exposure to airborne germs—perfect for added peace of mind during cold and flu season!

SpeedySwab™ Rapid COVID-19 + Flu A&B Test

Committed to providing innovative diagnostic testing devices.

Watmind USA is a leading healthcare biotechnology company committed to providing innovative diagnostic testing devices to U.S. consumers. Our mission is to improve healthcare outcomes by delivering reliable, fast, and accurate testing solutions. At the heart of this mission is our flagship brand, SpeedySwab™, which sets the standard for COVID-19 Flu A + B test innovation. By prioritizing accuracy, speed, and convenience, SpeedySwab™ ensures that individuals and healthcare providers have access to the most efficient at-home COVID flu test and COVID flu self-test options on the market.

Frequently asked questions

Find clear, helpful answers to the most common questions about SpeedySwab™ Rapid COVID-19 + Flu A&B Test.

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The test uses lateral flow immunochromatographic technology to detect and differentiate between the antigens of COVID-19, Flu A, and Flu B from a nasal swab sample. Results are available in 15 minutes.

The test is intended for use by healthcare professionals for in-vitro diagnostic purposes. It is used for individuals showing symptoms of respiratory infections within the first five days of symptom onset.

The test has a shelf life of up to 18 months. Check the expiration date on the box before use.

The test has a clinical sensitivity of 92.6% for COVID-19, 82.9% for Flu A, and 90% for Flu B.

This test is authorized by the FDA under Emergency Use Authorization (EUA). It is not FDA approved or cleared, but it is authorized for the detection of SARS-CoV-2, influenza A, and influenza B.