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INDICAID COVID-19 Rapid Antigen Test (FDA EUA, CE) is a lateral flow immunoassay designed for the qualitative detection of SARS-CoV-2 antigens in direct nasal swab samples.
Product Benefits Fast: Intuitive visual results in 20 minutes Accurate : Clinically validated with overall sensitivity and specificity at 96% and 99.9% respectively Easy-to-Use: No special equipment or facilities needed Developed in Hong Kong: With reliable product quality Product Certification: The first COVID-19 product in Greater China that has obtained US FDA EUA and EU CE mark Variants detectability: Able to detect the presence of certain COVID-19 variants*
*Detectable variants include Alpha (B.1.1.7), Beta (B.1.351), Gamma (P.1), Delta (B.1.617.2), Delta Plus (AY.1 and AY.2), and Omicron (B.1.1.529)
Instruction
1. Collect nasal swab sample 2. Mix sample into the buffer solution 3. Add the buffer solution into the sample well 4. Read the result after 20 minutes and no more than 25 minutes
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