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Abbott 2IDNOW15C Respiratory Test Kit, COVID-19 2.0 Molecular Diagnostic Rapid, 15 X 24 Tests, For ID Now Instrument US
Contents Include: (2) ID NOW Instruments (NAT024), (15) ID NOW COVID-19 2.0 Test Kits (192000)

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Item#: Abb-2IDNOW15C-EA
$18,859.31
Item(s) Total: $18,859.31
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  • Product Details
    • Dealer # 1249538
    Manufacturer # 2IDNOW15C
    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 (2) ID NOW Instruments (NAT024), (15) ID NOW COVID-19 2.0 Test Kits (192000)
    For Use With For ID Now™ Instrument US
    Number of Tests 15 X 24 Tests
    Product Dating McKesson Acceptable Dating: we will ship >= 90 days
    Purchase Program Type Promotion
    Reading Type Machine Read
    Sample Type Nasal Swab / Nasopharyngeal Swab Sample
    Specialty Molecular
    Technology Isothermal Nucleic Acid Amplification Technology (NAAT)
    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)
    UNSPSC Code 41116144

    Features

    • )ID NOW Promotion: (15) COVID-19 2.0 Kits (427000) + (2) each ID NOW instrument (NAT024)
    • 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
    • Each COVID-19 2.0 Kit contains: (24) Test Bases, (24) Sample Receivers, (24) Transfer Cartridges, (24) Nasal Swabs, Positive and Negative Control Swabs, Product Insert and Quick Reference Instructions
    • 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
    • Unique ID NOW™ Instrument isothermal nucleic acid amplification technology provides molecular results in just minutes, allowing you to make effective clinical decisions sooner
    • A key new feature of the ID NOW COVID-19 510(k) product and the supporting software update v7.1 provides customers with the flexibility to use a new sequential testing workflow; the sequential workflow will allow customers to have the option to add-on an ID NOW Influenza A & B 2 test after a COVID-19 result is received, using the same patient sample
    • The new sequential testing workflow feature and the updated 510(k) labeling will apply to existing ID NOW COVID-19 2.0 EUA product after upgrading to software update v7.1; by performing this software update, it enables the sequential workflow for any ID NOW COVID-19 2.0 EUA product you may have in inventory
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