Status COVID-19 / Flu A and B Rapid Antigen Test Kit - 25 Tests

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  • Simultaneous detection of COVID-19, Flu A, and Flu B antigens
  • Rapid 15-minute visual results without specialized equipment
  • FDA Emergency Use Authorization for professional settings
  • High sensitivity and specificity across all three pathogens
  • Complete kit with all necessary components for 25 tests
  • Flocked nasopharyngeal swabs for optimal specimen collection
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Price: $438.99

HSA/FSA Eligible

Pay with your health savings account

Subject to guarantee terms (one claim per customer/year). How does this work?

No refunds, exchanges or returns
FREE Shipping on orders $79+
Sold out

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  • Simultaneous detection of COVID-19, Flu A, and Flu B antigens
  • Rapid 15-minute visual results without specialized equipment
  • FDA Emergency Use Authorization for professional settings
  • High sensitivity and specificity across all three pathogens
  • Complete kit with all necessary components for 25 tests
  • Flocked nasopharyngeal swabs for optimal specimen collection

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Status COVID-19 / Flu A and B Rapid Antigen Test Kit

This comprehensive 25-test kit provides rapid, simultaneous detection of COVID-19, Influenza A, and Influenza B antigens from nasopharyngeal swab specimens. Designed for professional healthcare settings, this FDA EUA-authorized test delivers reliable results in just 15 minutes.

Professional-Grade Respiratory Testing

Each kit contains everything needed for 25 individual tests, including test devices, extraction reagent capsules, sterile swabs, and control swabs for quality assurance. The convenient packaging ensures proper storage and easy access for healthcare professionals.

Key Performance Characteristics

  • COVID-19: 93.9% Sensitivity, 100% Specificity
  • Influenza A: 91.4% Sensitivity, 95.7% Specificity
  • Influenza B: 87.6% Sensitivity, 95.9% Specificity

Intended Use and Applications

This lateral flow immunoassay is designed for the qualitative detection and differentiation of nucleocapsid antigens from SARS-CoV-2, influenza A, and influenza B. It is intended for use within the first five days of symptom onset in individuals suspected of respiratory viral infection.

The test utilizes flocked nasopharyngeal swabs for superior specimen collection and patient comfort. No specialized analyzer or reader is required – results are determined through visual interpretation, making it suitable for various healthcare settings operating under CLIA certification.



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