LumiraDx SARS-CoV-2 Antigen Test Kit - 48 Tests

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  • Rapid 12-minute results from sample application
  • CLIA-waived for point-of-care settings
  • Microfluidic immunofluorescence assay technology
  • Simple workflow with instrument guidance
  • 48 individually packed test strips included
  • Emergency use authorized for SARS-CoV-2 detection
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Price: $1,622.99

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No refunds, exchanges or returns
FREE Shipping on orders $79+
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  • Rapid 12-minute results from sample application
  • CLIA-waived for point-of-care settings
  • Microfluidic immunofluorescence assay technology
  • Simple workflow with instrument guidance
  • 48 individually packed test strips included
  • Emergency use authorized for SARS-CoV-2 detection

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LumiraDx SARS-CoV-2 Antigen Test Kit - 48 Tests

This comprehensive 48-test kit provides rapid antigen detection for SARS-CoV-2 using the advanced LumiraDx platform. Designed for professional healthcare settings, this CLIA-waived test delivers reliable results in just 12 minutes from sample application.

Rapid and Accurate Testing Solution

The LumiraDx SARS-CoV-2 Ag Test utilizes microfluidic immunofluorescence assay technology to detect SARS-CoV-2 nucleocapsid protein antigens in nasal swab specimens. This test is authorized for emergency use and is suitable for point-of-care settings operating under CLIA certification.

Complete Kit Contents

  • 48 individually packed test strips
  • LumiraDx test product insert
  • RFID tag for instrument compatibility
  • Dropper lids for sample application
  • Quick reference instructions

Professional Use Requirements

This test is intended for use by trained clinical laboratory personnel and individuals proficient in performing tests using the LumiraDx Instrument. The workflow features simple sample preparation with step-by-step guidance from the instrument to ensure consistent, reliable results.

Positive results indicate the presence of viral antigens and should be correlated with patient history and other diagnostic information. Negative results should be considered in the context of clinical signs, symptoms, and exposure history, with molecular assay confirmation when necessary.



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