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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

Frequently asked questions

Does this test provide rapid molecular results?
<p>Yes, it utilizes <strong>isothermal technology</strong> to deliver results significantly faster than traditional PCR methods. You can expect positive results in as little as <strong>6 minutes</strong> and negative results in just <strong>12 minutes</strong>.</p>
Is this kit easy to use for staff?
<p>Absolutely. It is designed for simplicity in high-throughput environments and features: &lt;ul&gt;&lt;li&gt;<strong>Video-guided on-screen operation</strong>&lt;/li&gt;&lt;li&gt;Elimination of manual pipetting&lt;/li&gt;&lt;li&gt;Minimal training requirements&lt;/li&gt;&lt;/ul&gt;</p>
Can I test for other respiratory illnesses simultaneously?
<p>Yes, the system supports <strong>diagnostic stewardship</strong>. Clinicians have the flexibility to add on <strong>Influenza A &amp; B testing</strong> using the same patient sample, which streamlines the diagnostic process and reduces patient discomfort.</p>
Does the kit require specialized storage conditions?
<p>No, the kit is designed for convenience and supports <strong>room temperature storage</strong> (between 2°C to 30°C), ensuring it is ready for on-demand use whenever clinical needs arise.</p>
What sample types are compatible with this test?
<p>The ID NOW COVID-19 2.0 test kit is compatible with two common sample collection methods: &lt;ul&gt;&lt;li&gt;<strong>Nasal Swab</strong>&lt;/li&gt;&lt;li&gt;<strong>Nasopharyngeal Swab</strong>&lt;/li&gt;&lt;/ul&gt;</p>
Are all necessary components included in the box?
<p>Yes, each kit contains 24 complete test sets. Included in your purchase are: &lt;ul&gt;&lt;li&gt;24 Test Bases, Sample Receivers, and Transfer Cartridges&lt;/li&gt;&lt;li&gt;Patient Swabs&lt;/li&gt;&lt;li&gt;Positive and Negative Control Swabs&lt;/li&gt;&lt;li&gt;Package Insert and Quick Reference Instructions&lt;/li&gt;&lt;/ul&gt;</p>
Is this system classified as CLIA-waived?
<p>Yes, this product is <strong>CLIA-waived</strong>, making it an excellent choice for point-of-care settings like urgent care centers and professional clinics that require regulatory compliance and ease of operation.</p>
What hardware is required to run these tests?
<p>To perform these tests, you must have the <strong>ID NOW Instrument</strong>. Please note that the instrument is sold separately from this test kit.</p>