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8 In 1 SARS-CoV-2/Flu A+B/HPIV2/HPIV1+3/RSV/ADV/MP Antigen Rapid Test Kit

  • Immunochromatographic and Double-antibody Sandwich Method.
  • Detect SARS-CoV-2/Flu A+B/HPIV2/HPIV1+3/RSV/ADV/MP from human Oropharyngeal Swabs.
  • IVD CE Approved.
  • Valid for 24 Months.
  • WHOLESALE SUPPLY.
8IN1 Test:
Availability:
Quantity:
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  • ICA2114-15E

  • Bioteke

  • ICA2114-15E2024R1201

SARS-CoV-2/Flu A+B/HPIV2/HPIV1+3/RSV/ADV/MP Antigen Rapid Test Kit

(Immunochromatographic Assay)




INTENDED USE

Bioteke SARS-CoV-2/Flu A+B/HPIV2/HPIV1+3/RSV/ADV/MP Antigen Rapid Test Kit is used for the in vitro qualitative detection of Respiratory Multipathogen Antigen SARS-CoV-2/

Flu A+B/HPIV2/HPIV1+3/RSV/ADV/MP from human oropharyngeal swab specimens. 


Rapid and accurate diagnostic results can help determine the optimal timing for medication and treatment, reducing the risk of severe illness and monitoring the prognosis of respiratory diseases.


8 in 1 test kit features




PACKAGE SPECIFICATION

Components
Loading Quantity (Specification)
1 Test/Kit (1 box) 20 Tests/Kit (1 box)
Test card 
1pc
20pcs
Sample extraction tube
1pc 20pcs
Tube cap 1pc
20pcs
Swab 1pc 20pcs
Waste bag
1pc 20pcs


bioteke 8 in 1 test




PERFORMANCE CHARACTERISTICS

Bioteke SARS-CoV-2/Flu A+B/HPIV2/HPIV1+3/RSV/ADV/MP Antigen Rapid Test Kit

is an upgraded version with high sensitivity, specificity and total coincidence rate 99%.

  • SARS-CoV-2: sensitivity 94.24.77%, specificity 100%.

  • Influenza A: sensitivity 91.79%, specificity 100%.

  • Influenza B: sensitivity 90.84%, specificity 100%.

  • HPIV2: sensitivity 90.83%, specificity 100%.

  • HPIV1+3: sensitivity 89.74%, specificity 100%.

  • RSV: sensitivity 88.60%, specificity 100%.

  • ADV: sensitivity 91.87%, specificity 100%.

  • MP: sensitivity 90.18%, specificity 100%.


bioteke 8 in 1 ag test





OPERATION PROCESS GUIDE


test process

Remark:

  • Read the User Instruction carefully before testing.

  • Check the test kit validity and the contents to make sure that nothing is damaged or broken.

  • Please refer to the User Manul for test results interpretation.

  • The swab specimen should be tested immediately after collection.




APPLICABLE SCENARIO


Medical labs, Clinics, Basic medical institutions / At home self-testing, etc.


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