SARS-CoV-2 ANTIGEN RAPID TEST KIT LOT OF 100

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1. Easy to gather The Latest Info Found Here without expert devices. 2. The test results are available in 15 minutes, and the test results are clearly visible. 3. Convenient transport and low cost, greater accuracy. 4. Suitable for large-scale rapid screening.

COVID-19 Rapid Test Kit IgG + IgM (Colloidal Gold) (A122152)

The Food and Drug Administration (FDA) has warned consumers to stop using an unapproved COVID-19 at-home rapid test and antibody test over concerns that the packages might produce incorrect results. The sets, produced by Lepu Medical Technology, were dispersed to drug stores to be sold to customers for at-home testing and provided through direct sales regardless of not having FDA permission.

The FDA said it has "severe concerns about the performance" of both tests. Healthcare companies who used the antigen test within the last two weeks and suspect an incorrect outcome are encouraged to retest clients using a different package. Those who utilized the antibody test just recently and suspect a false result are likewise advised to retest clients utilizing a different package.

SARS-Co, V-2 Antigen Quick Test Package (Colloidal Gold)20 Tests/box (1Test/bag 20 Bags),40 Tests/box (1Test/bag 40 Bags)INTENDED USEFor in vitro qualitative detection of SARS-Co, V-2 nucleocapsidantigen in nasal (NS) swab specimens directly from people who are suspected of COVID-19 by their doctor within the very first 5 days after onset of symptoms.

COVID-19 IgG/IgM Rapid Test Kit (Colloidal Gold) - JOYSBIO Biotechnology

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Severe severe breathing syndrome coronavirus 2 (SARS-Co, V-2, or 2019-n, Co, V) is an enveloped non-segmented positive-sense RNA virus. It is the cause of coronavirus illness (COVID-19), which is contagious inhumans. SARS-Co, V-2 has numerous structural proteins consisting of spike (S), envelope (E), membrane (M), and nucleocapsid (N). The antigen is normally noticeable in upper respiratory samples throughout the intense phase of infection.

Favorable results do not eliminate a bacterial infection or co-infection with other viruses. The agent detected might not be the certain cause of illness. Unfavorable results ought to be treated as presumptive, which do not eliminate SARS-Co, V-2 infection and should not be used as the sole basis for treatment or patient management decisions, including infection control decisions.