COVID-19 rapid test
for antibodiesSARS-COV-2serum

COVID-19 rapid test - LumiraDx - for antibodies / SARS-COV-2 / serum
COVID-19 rapid test - LumiraDx - for antibodies / SARS-COV-2 / serum
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COVID-19 rapid test - LumiraDx - for antibodies / SARS-COV-2 / serum - image - 3
COVID-19 rapid test - LumiraDx - for antibodies / SARS-COV-2 / serum - image - 4
COVID-19 rapid test - LumiraDx - for antibodies / SARS-COV-2 / serum - image - 5
COVID-19 rapid test - LumiraDx - for antibodies / SARS-COV-2 / serum - image - 6
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Characteristics

Applications
COVID-19
Tested parameter
for antibodies
Micro-organism
SARS-COV-2
Sample type
serum, plasma, whole blood, clinical
Analysis mode
immunofluorescence
Format
strip
Result display time

11 min

Sensitivity

Max.: 100 %

Min.: 84.6 %

Description

The LumiraDx SARS-CoV-2 Ab Test is a microfluidic immunofluorescence assay for qualitative detection of total antibodies to SARS-CoV-2 in human whole blood (capillary fingerstick or venous), plasma or serum for indication of recent or prior infection. Used with the LumiraDx Platform the Test delivers rapid results at the point of care. Test benefits The LumiraDx SARS-CoV-2 Ab Test is designed to be used in community care settings to identify individuals with an adaptive immune response to COVID-19, indicating recent or prior infection. Easy to implement in point of care settings Clinical agreement (direct fingerstick) in samples collected more than 8 days post RT-PCR 100% (62/62) positive agreement 100% (54/54) negative agreement Test procedure The Instrument and Test Strips are integrated with several quality control checks to ensure the Instrument and Test are functioning correctly for every test run. The workflow process is comprised of a simple sample collection with a fingerstick lancet followed by step-by-step guidance of the Instrument to report a patient result in 11 minutes from sample application. Test performance Fingerstick sample performance In clinical studies, fingerstick samples showed 100% positive agreement and 100% negative agreement when collected more than 8 days post RT-PCR. Plasma sample performance In clinical studies, plasma samples demonstrated an overall 97.2% positive agreement and 100% negative agreement when compared to RT-PCR.

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