Carestart COVID-19 Rapid Antigen Tests (20 included)
BOX INCLUDES THE FOLLOWING:
20 Tests/Kits
20 Assay buffer
20 Extraction vials and caps
20 Specimen collection swabs
1 Positive and 1 Negative control swabs
1 Instruction for Use
FEATURES:
Lateral flow assay
Rapid results in 10 minutes
Nasopharyngeal specimen collection
Intended at POC setting (i.e., in patient care settings) by medical professionals
CLINICAL FEATURES:
Detect SARS-CoV-2 nucleocapsid protein antigen
Indentify acute infection with 88.4% sensitivity and 100% specificity
DUE TO HIGH DEMAND, PLEASE ALLOW UP TO 10 DAYS FOR DELIVERY
BOX INCLUDES THE FOLLOWING:
20 Tests/Kits
20 Assay buffer
20 Extraction vials and caps
20 Specimen collection swabs
1 Positive and 1 Negative control swabs
1 Instruction for Use
FEATURES:
Lateral flow assay
Rapid results in 10 minutes
Nasopharyngeal specimen collection
Intended at POC setting (i.e., in patient care settings) by medical professionals
CLINICAL FEATURES:
Detect SARS-CoV-2 nucleocapsid protein antigen
Indentify acute infection with 88.4% sensitivity and 100% specificity
DUE TO HIGH DEMAND, PLEASE ALLOW UP TO 10 DAYS FOR DELIVERY
BOX INCLUDES THE FOLLOWING:
20 Tests/Kits
20 Assay buffer
20 Extraction vials and caps
20 Specimen collection swabs
1 Positive and 1 Negative control swabs
1 Instruction for Use
FEATURES:
Lateral flow assay
Rapid results in 10 minutes
Nasopharyngeal specimen collection
Intended at POC setting (i.e., in patient care settings) by medical professionals
CLINICAL FEATURES:
Detect SARS-CoV-2 nucleocapsid protein antigen
Indentify acute infection with 88.4% sensitivity and 100% specificity
DUE TO HIGH DEMAND, PLEASE ALLOW UP TO 10 DAYS FOR DELIVERY
The CareStart COVID-19 ANTIGEN TEST is a lateral flow immunochromatographic assay for rapid detection of extracted nucleocapsid protein antigens specific to SARS-CoV-2 in swab specimens directly collected from symptomatic individuals who are suspected of COVID-19 by their healthcare providers. No additional equipment or instruments are required for this test.
Additional Information
FDA Emergency Use Authorization Information