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COVID-19 is an acute respiratory infectious disease. People are generally susceptible. Currently, the patients infected by the novel corona-virus are the main source of infection; asymptomatic infected people can also be an infectious source. Based on the current epidemiological investigation, the incubation period is 1 to 14 days, mostly 3 to 7 days. The main manifestations include fever, fatigue and dry cough. Nasal congestion, runny nose, sore throat, myalgia and diarrhea are found in a few cases.

FRENOVO FLU A+B & COIVD-19 antigen rapid test qualitatively detects the presence of Influenza A and/or Influenza B antigen in nasal swab or throat swab or nasal aspirate specimens, providing results within 15 minutes.

The Novel Corona-viruses Belong To The β Genus of COVID-19 Ag Test

COVID-19 is an acute respiratory infectious disease. People are generally susceptible. Currently, the patients infected by the novel corona-virus are the main source of infection; asymptomatic infected people can also be an infectious source. Based on the current epidemiological investigation, the incubation period is 1 to 14 days, mostly 3 to 7 days. The main manifestations include fever, fatigue and dry cough. Nasal congestion, runny nose, sore throat, myalgia and diarrhea are found in a few cases.

FRENOVO FLU A+B & COIVD-19 antigen rapid test qualitatively detects the presence of Influenza A and/or Influenza B antigen in nasal swab or throat swab or nasal aspirate specimens, providing results within 15 minutes.

Test Principle of COVID-19 Ag Test

COVID-19 Ag Rapid Test is designed to detect antigen from the SARS-CoV-2 in human nasopharyngeal swab specimens from patients who are suspected of COVID-19 by their healthcare provider within the first seven days of symptom onset, or from individuals without symptoms or other epidemiological reasons to suspect COVID-19 when tested twice over two or three days with at least 24 hours and no more than 48 hours between tests. The Celltrion DiaTrustTM COVID-19 Ag Rapid Test is validated for use from direct specimens testing without transport media.

Quality Control of COVID-19 Ag Test

An external positive control is needed to confirm that the device performs as intended and that the test procedure is conducted correctly. 0.1 μg/mL of non-infectious recombinant SARS-CoV-2 RBD antigen and 0.1 μg/mL non-infectious recombinant SARS-CoV-2 nucleoprotein antigen is dried onto the swab. This control swab should be tested once with every new lot and shipment, on a daily basis, for each new user, or according to the quality control procedures established for each laboratory.

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