WellLife WV01P0002 COVID-19 / Influenza A&B Combo Rapid Test
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COVID-19 / Influenza A&B Combo Rapid Test Kit POC Box of 25

SKU: MD836206
MFG Part#: WV01P0002
In Stock

Usually ships in 5 - 10 Days

Sale:

$159.99

25 / Kit
was $350.00
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What's In The Box:
  • (25) Combo Flu-A, Flu-B, and COVID-19 Tests
  • Prefilled extraction buffer
  • Sterile swabs
  • Positive control swab
  • Negative control swab
  • Tube holder
  • Package insert
  • Quick Reference Instruction
Description

The WELLLIFE™ COVID-19 / Influenza A&B Test is a cutting-edge point-of-care diagnostic tool designed for rapid and accurate detection of COVID-19 and influenza A and B viruses. Ideal for use in clinical settings, this test provides reliable results within 10 minutes, allowing healthcare providers to make swift and informed decisions. With an extended detection window and built-in quality assurance features, it is a vital resource for managing viral infections effectively.

Features
  • Cost-effective: Efficiently screen for three types of antigens with one test kit.
  • Rapid Results: Obtain test results within 10 minutes, aiding in immediate decision-making for patient care.
  • Quality Assurance: Built-in controls ensure reliable performance and clinical accuracy.
  • Extended Detection Window: Detect antigens up to five days after symptom onset.
  • Wide Storage Temperature: Easy storage between 36°F-86°F (2°C-30°C) for flexible inventory management.
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Product Specifications
Items Per Box: 25
Specimen Type: Nasal Swab
Result Time: 10 Minutes
SARS-COV-2 Positive Percent Agreement (PPA): 87.5%
Influenza A Positive Percent Agreement (PPA): 85.9%
Influenza B Positive Percent Agreement (PPA): 86.8%
Negative Percent Agreement (NPA): 99.7%
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Frequently Asked Questions (FAQs)
The test can be stored between 36°F-86°F (2°C-30°C), making it convenient for various healthcare settings.
Results are available in just 10 minutes, allowing for immediate testing and treatment decisions during the same office visit.
Yes, this product has been authorized by the FDA under Emergency Use Authorization (EUA) for the detection of SARS-CoV-2, influenza A, and influenza B antigens.
The test shows high Positive Percent Agreement (PPA) and Negative Percent Agreement (NPA) percentages, ensuring reliable diagnostic accuracy.
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