SpeedySwab™ Rapid Antigen Test, COVID-19 + Flu A&B, 25 Test-Pack

Fast, Reliable In-Clinic Testing for COVID-19 & Flu

The SpeedySwab™ Rapid COVID-19 + Flu A&B Antigen Test is a point-of-care (POC) diagnostic tool designed for healthcare providers and organizations to rapidly differentiate between COVID-19, Influenza A, and Influenza B. This test provides accurate results in just 15 minutes, supporting efficient batch testing and quick clinical decision-making in a variety of healthcare settings.

Key Features:

Dual Detection: Differentiates between COVID-19, Flu A, and Flu B with a single test.

Fast & Reliable: Results in just 15 minutes for quick action.

Simple Workflow: Nasal swab sample with a streamlined process for minimal disruption.

Designed for Providers: Optimized for in-clinic testing and batch processing.

25-Test Pack: Suitable for high-volume testing environments.

Up to 15-Month Shelf Life: Ensures long-term availability.

Who is the SpeedySwab™ Rapid Antigen Test For?

Individuals with signs and symptoms of respiratory infection consistent with COVID-19 within the first five days of symptom onset. The 25 Test-Pack is designed for healthcare facilities, urgent care clinics, hospitals, and occupational health programs needing a fast, on-site testing solution.

More Information About the SpeedySwab™ POC Test

• How does the SpeedySwab™ Rapid COVID-19 + Flu A&B Test work?

  SpeedySwab™ is a lateral flow antigen test that detects and differentiates COVID-19, Influenza A, and Influenza B proteins using a simple nasal swab sample. The test provides results in just 15 minutes.

• Who can administer this test?

  This test is intended for use by healthcare professionals in point-of-care settings, such as clinics, hospitals, and urgent care centers.

• How soon will results be available?

  Results are ready in 15 minutes, allowing for fast clinical decision-making.

• How accurate is the test?

  The test has been clinically validated with the following sensitivity rates:

  • COVID-19: 92.6%

  • Flu A: 82.9%

  • Flu B: 90%

• How is this test different from the OTC version?

  • The POC version is designed for in-clinic, provider-administered testing.

  • It is available in a 25-test pack for batch processing.

  • It is authorized for use in healthcare settings under FDA EUA (#EUA230037).

• Is the SpeedySwab™ test FDA authorized?

  Yes, the test has received Emergency Use Authorization (EUA #EUA230037) from the U.S. FDA for use in point-of-care settings.

• What is the shelf life of the test?

  The SpeedySwab™ POC test has a shelf life of up to 15 months, ensuring it remains available when needed.

• What if I need a test for home use?

  The SpeedySwab™ Rapid COVID-19 + Flu A&B Test is also available as an over-the-counter (OTC) kit for home use. Learn more ⟩⟩

Downloadable Resources