Wondfo COVID-19 antibody rapid test has been approved!
February 24,2020 (Edit)
On Feb 22nd 2020, Wondfo One Step COVID-19 Antibody Test (Immunochromatography Assay) developed by Wondfo has successfully received CFDA certificate approved by National Medical Products Administration.
Designed for qualitative detection of 2019-nCoV antibodies in human serum, plasma, and whole blood samples, novel coronavirus  antibody detection reagent (Colloidal Gold Method) is regarded as auxiliary detection metrics towards on-site screening for suspected cases that have the negative results after nucleic acid testing. This rapid test can aid in the diagnosis of coronavirus infection and significantly shorten the detection time, yielding the results in 15 minutes.