Sale price$1,606.62
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Description

  • FDA-cleared ID NOW COVID-19 2.0 detects SARS-CoV-2 in 6–12 minutes with the option to add on the ID NOW Influenza A & B 2 test without collecting another sample
  • Product ships with minimum 30 days dating
  • Highly accurate, rapid molecular COVID-19 test
  • The ID NOW platform uses isothermal technology to provide molecular results faster than PCR for more timely and informed clincial decisions
  • CLIA-waived; requires minimum training with easy on-screen video-guided operation and no manual pipetting required
  • ID NOW Platform gives you the power to decide which tests to run based on patient presentation, circulating prevalence and seasonality of infectious diseases
  • Easily add on Flu A & B testing based on clinical necessity, supporting diagnostic stewardship
  • Diagnostic Stewardship: Right tests at the right time for optimal care and fewer unnecessary tests
  • Room temperature storage - run tests on demand, right out of the box
  • For use with the ID NOW Instrument
  • Materials required but not provided: ID NOW Instrument

Product Specs

Item Number 1232210
Catalog Number 192000
UOM KT
Level 1 Family Description Lab-Waived Lab
Level 2 Category Description Lab-Respiratory Testing
Level 3 Group Description COVID Testing
Level 4 Sub-Category Description COVID - Molecular
Application Respiratory Test Kit
Brand ID NOW
Buy American Act (BAA) Compliant Yes
CLIA Classification CLIA Waived
CLIA Classified CLIA Waived
Contents 1 (24) Test Bases, Sample Receivers, Transfer Cartridges, Patient Swabs, Positive Control Swab, Negative Control Swab, Package Insert, Quick Reference Instructions
Country of Origin United States
For Use With For ID NOW Instrument
Is_ECAT N
Is_GSA Y
Is_VA N
Manufacturer Abbott Rapid Dx North America LLC
Manufacturer # 192000
McKesson # 1213540
Number of Tests 24 Tests
Purchase Program Type Standard Purchase
Reading Type Machine Read
Sample Type Nasal Swab / Nasopharyngeal Swab Sample
Specialty Molecular
Technology Molecular (NAAT) Isothermal Technology
Test Format Cartridge Format
Test Kit Type Rapid
Test Name COVID-19 2.0
Test Type Molecular Diagnostic
Time to Results 6 Minute Results (Positive), 12 Minute Results (Negative)
Trade Agreement Act (TAA) Compliant Yes
UNSPSC Code 41116144