Product Description
Authorized for use at the Point of Care (POC)
The Rapid Response™ Liberty COVID-19 IgG/IgM is an immunochromatographic lateral flow assay intended for the qualitative detection and differentiation of Immunoglobulin M (IgM) and Immunoglobulin G (IgG) antibodies to SARS-CoV-2 in human serum, plasma (sodium citrate, sodium heparin, or dipotassium EDTA), venous whole blood (sodium citrate, sodium heparin, or dipotassium EDTA) and fingerstick whole blood. The Rapid Response™ Liberty COVID-19 IgG/IgM is intended for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection. At this time, it is unknown for how long antibodies persist following infection and if the presence of antibodies confers protective immunity. The Rapid Response™ Liberty COVID-19 IgG/IgM should not be used to diagnose or exclude acute SARS-CoV-2 infection.
- 25 Test Devices
- 1 Assay Buffer Bottle
- 25 Blood Transfer Pipettes
- 1 Package Insert
Product Description
Authorized for use at the Point of Care (POC)
The Rapid Response™ Liberty COVID-19 IgG/IgM is an immunochromatographic lateral flow assay intended for the qualitative detection and differentiation of Immunoglobulin M (IgM) and Immunoglobulin G (IgG) antibodies to SARS-CoV-2 in human serum, plasma (sodium citrate, sodium heparin, or dipotassium EDTA), venous whole blood (sodium citrate, sodium heparin, or dipotassium EDTA) and fingerstick whole blood. The Rapid Response™ Liberty COVID-19 IgG/IgM is intended for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection. At this time, it is unknown for how long antibodies persist following infection and if the presence of antibodies confers protective immunity. The Rapid Response™ Liberty COVID-19 IgG/IgM should not be used to diagnose or exclude acute SARS-CoV-2 infection.
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Canada