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COVID-19 Antigen Rapid Test Device

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COVID-19 Antigen Rapid Test Device

Sku: M3-COV2-RRTK

The COVID-19 Antigen Rapid Test Device allows for an efficient and cost-friendly method of detection. In just 15 minutes, the test can detect the SARS-CoV-2 viral nucleoprotein antigen through visual interpretation of colour development. The test is intended for use with Nasal and Nasopharyngeal swab specimens within 6 days of symptom onset.

 

**This product is out of stock. We recommend the Artron COVID-19 Antigen Rapid Test Device instead, as it serves the same/similar purpose as the Rapid Response Test Device

 

$495

Box Size:

This Product Is Out Of Stock

Antigen
COVID

description

The Rapid Response COVID-19 Antigen Rapid Test Device is an in vitro immunochromatographic assay for the direct and qualitative detection of SARS-CoV-2 viral nucleoprotein antigens from nasal and nasopharyngeal secretions from individuals suspected of COVID-19 within 6 days of symptom onset.

 

Results are for the identification of SARS-CoV-2 viral nucleoprotein antigen. Antigen is generally detectable in nasopharyngeal and nasal secretions during the acute phase of infection. Positive results indicate the presence of viral antigens, but clinical correlation with patient 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.

 

The agent detected may not be the definite cause of disease. Laboratories are required to report all positive results to the appropriate public health authorities. Negative results should be treated as presumptive, and 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.

 

Negative results should be considered in the context of a patient’s recent exposures, history, and the presence of clinical signs and symptoms consistent with COVID-19, and confirmed with a molecular assay, if necessary, for patient management.

 

Pursuant to section 5 of the Interim Order Respecting the Importation and Sale of Medical Devices for Use in Relation to COVID-19, made by the Minister of Health on March 18, 2020, the Rapid Response COVID-19 Antigen Rapid Test Device is now authorized for sale or importation in Canada.

 

Contents

  • Individually Packed Test Devices
  • Extraction Buffer
  • Extraction Tube
  • Nozzle with Filter
  • Tube Stand
  • Individually Packed Swabs
  • Package Insert

 

Details

  • Sample: Nasal / Nasopharyngeal secretions
  • Format: Cassette
  • Quantity: 25 Tests/Kit
  • Time To Result: 15 minutes
  • Storage Condition: 2-30°C/36-86°F
  • Test Principle: Immunochromatographic Assay

 

Users

  • The test is for in vitro diagnostic use for professional and self-testing purposes
  • These tests are for use by laboratory or healthcare professionals, in addition to home testing (or self-testing)
  • The Rapid Response® COVID-19 Antigen Rapid Test Device is authorized for use with nasal and nasopharyngeal secretions

 

Self-Testing 

Note: Each Province/Territory has different guidelines for Self-Testing, we encourage you to consult with your regulatory body before purchasing

  • View the video above or see here for a demonstration on how to perform a COVID-19 Antigen Rapid Test

 

EACH or BOX
25 Tests/Kit BOX

Contents:

  • Individually Packed Test Devices
  • Individually Packed Swabs
  • Tube Stand
  • Extraction Tube
  • Extraction Buffer
  • Nozzle with Filter
  • Package Insert

 


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