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Abbott Rapid Dx North America LLC Respiratory Test Kit ID NOW™ Molecular Diagnostic Respiratory Syncytial Virus Test (RSV) Nasopharyngeal Swab Sample 24 Tests CLIA Waived - KT/1 - 435000-KT

Abbott Rapid Dx North America LLC Respiratory Test Kit ID NOW™ Molecular Diagnostic Respiratory Syncytial Virus Test (RSV) Nasopharyngeal Swab Sample 24 Tests CLIA Waived - KT/1 - 435000-KT

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Abbott Rapid Dx North America LLC Respiratory Test Kit ID NOW™ Molecular Diagnostic Respiratory S...

Item Id 1038861
MF Id# 435000
Brand ID NOW™
Manufacturer Abbott Rapid Dx North America LLC
Country of Origin United States
Application Respiratory Test Kit
CLIA Classification CLIA Waived
CLIA Classified CLIA Waived
Contents 1 Test Base, Sample Receiver, Transfer Cartridge, Sterile Nasopharyngeal Swab, Positive Control Swab, Negative Control Swab, Plastic Disposable Pipette, Package Insert, Quick Reference Instructions
For Use With For ID Now™ Instrument US
Number of Tests 24 Tests
Product Dating McKesson Acceptable Dating: we will ship >= 90 days
Purchase Program Type Standard Purchase
Reading Type Machine Read
Sample Type Nasopharyngeal Swab Sample
Specialty Molecular
Test Name Respiratory Syncytial Virus Test (RSV)
Test Type Molecular Diagnostic
Time to Results 15 Minute Results
UNSPSC Code 41116144

Features

  • ID NOW™ RSV detects the RSV virus in nasopharyngeal (NP) swab samples using Alere’s proprietary Molecular In Minutes™ isothermal nucleic acid amplification technology (iNAT)
  • ID NOW™ i RSV is a rapid (less than 15 minutes), instrument-based isothermal test for the qualitative detection of RSV A and RSV B from nasopharyngeal swabs and nasopharyngeal swabs eluted in viral transport media
  • It is comprised of a Sample Receiver, containing elution buffer, a Test Base, comprising two sealed reaction tubes, each containing a lyophilized pellet, a Transfer Cartridge for transfer of the eluted sample to the Test Base
  • The reaction tubes in the Test Base contain the reagents required for amplification of RSV A and RSV B, respectively, as well as an internal control
  • Intended for use as an aid in the diagnosis of RSV in children <18 years and adults ≥60 years in conjunction with clinical and epidemiological risk factors
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