Respiratory Solutions

Helping Providers Manage Acute Respiratory Tract Infections

QDx provides molecular respiratory syndromic panels to support your clinical decision making when managing seasonal acute respiratory tract infections. Testing is based on accurate, rapid and reliable FDA approved methodologies so you can start patient treatment sooner while maintaining responsible antibiotic stewardship.

QDx provides molecular respiratory syndromic panels to support your clinical decision making when managing seasonal acute respiratory tract infections. Testing is based on accurate, rapid and reliable methodologies so you can start patient treatment sooner while maintaining responsible antibiotic stewardship.


Turn Around Time — 24 hours

COVID-19

QDx Respiratory Panels provide the detection and identification of specific viral and bacterial nucleic acids from individuals exhibiting signs and symptoms of respiratory infection. The panel is used for the detection of the following respiratory pathogens:


Turn Around Time — 24 hours

RPP COMPLETE REPORT

Provides detection of Group A Streptococcus (Group A β-hemolytic Streptococcus, Strep A) in throat swab specimens from patients with signs and symptoms of pharyngitis.


Turn Around Time — 24 hours

GROUP A STREPTOCOCCUS

GROUP A STREP COMPLETE REPORT

A Complete Service Offering

RPP – Essential

TESTING PANEL INCLUDES

  • Influenza A:
    • Influenza A H1
    • Influenza A H1-2009pdm
    • Influenza A H3
  • Influenza B
  • Respiratory Syncytial Virus A/B (RSV)
  • Sars-COV-2

This is a qualitative multiplexed nucleic acid-based in vitro diagnostic test for the simultaneous detection and identification of nucleic acids from multiple viruses and bacteria extracted from nasopharyngeal swab (NPS) samples obtained from individuals with signs and/or symptoms of respiratory tract infection.

RPP – Extended

TESTING PANEL INCLUDES

Viruses

  • Adenovirus
  • Coronavirus (229E, HKU1, NL63, OC43)
  • Human Metapneumovirus A/B
  • Human Rhinovirus/ Enterovirus
  • Influenza A Including:
    • Influenza A H1
    • Influenza A H1-2009pdm
    • Influenza A H3
  • Influenza B
  • Parainfluenza 1
  • Parainfluenza 2
  • Parainfluenza 3
  • Parainfluenza 4
  • Respiratory Syncytial Virus A/B

Bacteria

  • Bordetella parapertussis (ptxP)
  • Chlamydia pneumoniae
  • Mycoplasma pneumoniae

The RP2.1 is a multiplexed nucleic acid test intended for the simultaneous qualitative detection and differentiation of nucleic acids from multiple viral and bacterial respiratory organisms, including nucleic acid obtained from Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) collected with a nasopharyngeal swabs (NPS) from an individual observed by a healthcare provider to have signs and/or symptoms of respiratory infection.