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VIS-IDNOW15CF |

Respiratory Test Kit ID NOW™ COVID-19 2.0 / Influenza A + B 2.0 7 X 24 COVID-19 Tests , 8 X 24 Flu A+B Tests

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About this item

  • 7 Covid kits + 8 Flu kits + ID NOW instrument
  • Product ships with minimum 30 days dating
  • ID NOW COVID-19 2.0 Assay is for use under an Emergency use Authorization Only: https://www.fda.gov/medical-devices/coronavirus-disease-2019-covid-19-emergency-use-authorizations-medical-devices/in-vitro-diagnostics-euas-molecular-diagnostic-tests-sa
  • ID NOW COVID-19 2.0 assay performed on the ID NOW Instrument is a rapid molecular in vitro diagnostic test utilizing an isothermal nucleic acid amplification technology (NAAT) intended for the qualitative detection of nucleic acid from SARS-CoV-2 in
  • Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. §263a, that meet the requirements to perform high, moderate or waived complexity tests
  • The ID NOW COVID-19 2.0 assay is authorized for use at the Point of Care (POC), i.e., in patient care settings operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation
  • Positive results are indicative of the presence of SARS-CoV-2 RNA; clinical correlation with patient history and other diagnostic information is necessary to determine patient infection status
  • Positive results do not rule out bacterial infection or co-infection with other viruses
  • Testing facilities within the United States and its territories are required to report all results to the appropriate public health authorities
  • Negative results should be treated as presumptive and, if inconsistent with clinical signs and symptoms or necessary for patient management, should be confirmed with a different authorized or cleared molecular test in a CLIA-certified laboratory that
  • Negative results do not preclude SARS-CoV-2 infection and should not be used as the sole basis for patient management decisions; negative results must be combined with clinical observations, patient history, and/or epidemiological information
  • To utilize the ID NOW COVID-19 2.0 assay, a software upgrade to version 7.0.0.20 is required for all instruments; the software upgrade is backward compatible to support use of ID NOW COVID-19, Influenza A & B 2, Strep A 2, and RSV inventory
  • ID NOW COVID-19 2.0 is intended for use by trained operators who are proficient in performing tests using the ID NOW Instrument
  • Price: Available Upon Quote

    50+ In Stock.

    PROMO PKG, ID NOW 7COVID/8FLU D/S
    Product Specifications:
    Manufacturer #: IDNOW15CF
    Brand: ID NOW™
    Manufacturer: Abbott Rapid Dx North America LLC
    Country of Origin: United States
    Application: Respiratory Test Kit
    Contents 1: ID NOW Instrument (NAT024), (7) ID NOW COVID-19 2.0 Test Kits (192000) (EUA), (8) ID NOW Influenza A/B 2.0 Kits (427000)
    For Use With: For ID Now™ Instrument US
    Number of Tests: 7 X 24 COVID-19 Tests , 8 X 24 Flu A+B Tests
    Purchase Program Type: Starter Kit
    Reading Type: Machine Read
    Sample Type: Nasal Swab / Nasopharyngeal Swab Sample
    Specialty: Molecular
    Technology: Isothermal Nucleic Acid Amplification Technology (NAAT)
    Test Format: Test Device Format
    Test Kit Type: Rapid
    Test Name: COVID-19 2.0 / Influenza A + B 2.0
    Test Type: Molecular Diagnostic
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    Please note that product and satisfaction concerns must be brought to our team's attention within (1) one-year from the date of purchase or within 50% of product usage (usually found in Printer Settings). Concerns made known after the one-year period will be issued store credit. We must receive the items being returned before we issue a refund or store credit.

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    • What is a compatible ink cartridge?
      A compatible ink or toner cartridge is a generic version of a name-brand cartridge. However, not all cartridges are made with the same quality. All Vivid Series cartridges pass a rigorous compliance test and are certified under the ISO 9001/14001 quality and environmental system. All Vivid Series branded cartridges include our Vivid Series lifetime satisfaction guarantee, a full 1-year warranty, and lifetime customer support.
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      MAGNUSON-MOSS WARRANTY IMPROVEMENT ACT

      United States Code Annotated

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      Chapter 50 Consumer Product Warranties

      Section 2302 (c)

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