SARS-CoV-2 Antigen Description
The Antigen Rapid Test Kit is an immunochromatographic assay that detects the nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal and nasal swab specimens rapidly. This can be done directly or after the swabs have been transported from suspected infected individuals.
This test is authorised for use at the Point of Care (POC), or patient care locations operating under CLIA Certificates.
Positive results do not rule out bacterial infection or co-infection with other viruses, and should not be used as the sole basis for treatment or SARS-CoV-2 patient management decisions.
Why buy SARS-CoV-2 Rapid Kit from us?
- Unique QR code on SARS-CoV-2 test cassettes
- CE Marked and FDA authorized under EUA Lateral Flow.
- Nasal samples.
- Simple usage, quick results.
- All accessories included.
- Simple to use and fast results.
- Usable for all ages from 2 to adult.
How to Store
Store at room temperatures (2-30°C).
What Do the Results Mean?
Positive result: Both T and C lines visible vividly or faintly.
Negative result: Only C line visible, T line not visible.
Invalid Result: Both T and C lines blank / not visible. Must retest.
Provided in the Package:
- Test cassettes.
- Individually wrapped specimen sampling sterile swab.
- Extraction tubes.
- Nozzle for extraction tubes.
- Bottle of sample extraction buffer.
- Instruction for use.
Performance Data
Sensitivity: 82.14% (23/28), in comparison with nucleic acid amplification test confirmed positive cases. Specificity: 99.45% (180/181), the negative cases were also confirmed by nucleic acid amplification test. Cross reactivity: There is no cross reactivity with influenza A virus, influenza B virus, adenovirus, Coxsackie virus, ECHO virus and enterovirus; no cross reactivity with Chlamydia pneumoniae, Mycoplasma pneumoniae, Chlamydia psittaci and Chlamydia trachomatis; no cross reactivity with Acinetobacter baumannii, Bordetella pertussis, Candida albicans, Escherichia coli, Haemophilus influenzae and Neisseria gonorrhoeae.

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