(25 Tests per Kit)
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For use with Sofia 2 - FDA Emergency Use Authorization
The Sofia 2 Flu + SARS Antigen Fluorescent Immunoassay (FIA) uses advanced immunofluorescence-based lateral flow technology in a sandwich design for qualitative detection of nucleocapsid protein from influenza A and influenza B, and SARS-CoV-2. The Sofia 2 Flu + SARS Antigen FIA with the Sofia 2 analyzer provides automated and objective results in 15 minutes, allowing for testing of patients suspected of influenza A, influenza B, and COVID-19/-nCoV at the Point of Care.
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DESCRIPTION
SARS-Cov-2&#;Influenza A&#;B Combo Rapid Test Cassette (swab) is an in vitro diagnostic test for the qualitative detection of novel coronavirus antigens and influenza A and B antigens in Nasopharyngeal swab, using the rapid immunochromatographic method. It will provide information for clinical doctors to prescribe correct medications.
The SARS-CoV-2 & Influenza A&B Combo Rapid Test Cassette is a diagnostic tool designed to simultaneously detect the presence of SARS-CoV-2 (the virus responsible for COVID-19) as well as Influenza A and Influenza B viruses. This test cassette offers a convenient and efficient method for healthcare professionals to identify and differentiate between these respiratory viruses in a single testing procedure.
The test cassette utilizes a lateral flow immunoassay technique, which detects specific viral antigens present in nasal or throat swab samples. It provides rapid results within a short span of time, usually within 10 to 20 minutes, enabling prompt decision-making for patient management and appropriate isolation measures.
By combining the detection of SARS-CoV-2 with Influenza A and B viruses, this test cassette offers a comprehensive approach to respiratory virus screening. It aids in distinguishing between different respiratory illnesses, ensuring accurate diagnoses, and guiding appropriate treatment strategies. This multi-pathogen approach is particularly valuable during flu seasons or outbreaks, where it becomes crucial to differentiate between COVID-19 and influenza cases due to the overlapping symptoms they may present.
SPECIFICATIONS
Contact us to discuss your requirements of nasal swab influenza test. Our experienced sales team can help you identify the options that best suit your needs.
INTENDED USE
This kit is intended for layperson's home use in a non-laboratory environment (e.g. in a person's residence or in certain non-traditional places such as offices, sporting events, airports, schools,l etc.).
&#;DIRECTIONS FOR USE&#;
1. Remove the test device from the sealed foil pouch and use it as soon as possible. Place the test device on a clean and level surface. Best results will be obtained if the assay is performed immediately after opening the foil pouch.
2. Take out the Extraction Tube.
3. Take out 1 bottle of Sample Extraction Buffer, remove the bottle cap, add all the extraction buffer into the extraction tube.
4. Place the sterilized swab specimen in the sample extraction buffer. Rotate the swab for approximately 10 seconds while pressing the head against the inside of the tube to release the antigen in the swab.
5. Remove the sterilized swab while squeezing the sterilized swab head against the inside of Buffer as you remove it to expel as much liquid as possible from the swab. Discard the sterilized swab in accordance with your biohazard waste disposal protocol.
6. Screw on and tighten the Nozzle with Filter onto the specimen collection tube, then shake the specimen collection tube vigorously to mix the specimen and the sample extraction buffer.
See illustration 4.
7. Add 3 drops of the solution (approx.80ul) to each sample well and then start the timer. Read the result at 10~20 minutes. Don&#;t interpret the result after 20 minutes.
Item Dimensions LxWxH : 0.00 x 0.00 x 0.00 Centimeters
Item Weight : 0.00KG
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