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VIS-11561909 |

Respiratory Test Kit Clinitest® At-Home OTC COVID-19 Test 800 Tests CLIA Waived

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About this item

  • The CLINITEST® Rapid COVID-19 Antigen Self-Test is only for use under the Food and Drug Administration’s Emergency Use Authorization: https://www.fda.gov/medical-devices/coronavirus-disease-2019-covid-19-emergency-use-authorizations-medical-devices/i
  • The CLINITEST® At-Home OTC COVID-19 Test is a lateral flow chromatographic immunoassay intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2
  • This test is authorized for non-prescription home use with self-collected anterior nasal (nares) swab samples from individuals aged 14 years or older with symptoms of COVID-19 within the first 7 days of symptom onset
  • This test is also authorized for non-prescription home use with adult-collected anterior nasal (nares) swab samples from individuals aged 2 years or older with symptoms of COVID-19 within the first 7 days of symptom onset
  • Results are for the identification of SARS-CoV-2 nucleocapsid protein antigen; antigen is generally detectable in anterior nasal (nares) swabs during the acute phase of infection
  • Positive results indicate the presence of viral antigens, but clinical correlation with past medical history and other diagnostic information is necessary to determine infection status
  • Positive results do not rule out bacterial infection or co-infection with other viruses
  • Individuals who test positive with CLINITEST® Rapid COVID-19 Antigen Self-Test should self-isolate and seek follow-up care with their physician or healthcare provider as additional testing may be necessary
  • Negative results should be treated as presumptive and confirmation with a molecular assay, if necessary, for patient management, may be performed
  • Negative results do not rule out SARS-CoV-2 infection and should not be used as the sole basis for treatment or patient management decisions, including infection control decisions
  • Individuals should provide all results obtained with this product to their healthcare provider for public health reporting
  • With the CLINITEST® Rapid COVID-19 Antigen Self-Test, you can expect accurate and reliable results in just 15 minutes
  • 200 4pk kits in a case or 800 total tests
  • Price: Available Upon Quote

    50+ In Stock.

    CLINITEST, COV19 AG HOME US ALBERTSON (4/KT 200KT/CS)
    Product Specifications:
    Manufacturer #: 11561909
    Brand: Clinitest®
    Manufacturer: Siemens
    Country of Origin: China
    Application: Respiratory Test Kit
    CLIA Classified: CLIA Waived
    Contents 1: Each Kit has: (4) Test Devices, (4) Sterile Swabs, (4) Extraction Tubes with Buffers and Tips, Instructions for Use
    Number of Tests: 800 Tests
    Purchase Program Type: Standard Purchase
    Reading Type: Visual Read
    Sample Type: Nasal Swab Sample
    Specialty: Immunoassay
    Test Format: Cassette Format
    Test Kit Type: Rapid
    Test Method: Lateral Flow Chromatographic Immunoassay
    Test Name: At-Home OTC COVID-19 Test
    Test Type: Antigen Detection
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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.

    Below you will find our most frequently asked questions. If you have any additional questions or feedback, please do not hesitate to contact us.

    • 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

      Title 15 Commerce and Trade

      Chapter 50 Consumer Product Warranties

      Section 2302 (c)

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