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Live Positive, Live with Faith...

Live Positive, Live with Faith...
Live Positive, Live with Faith...

SARS-CoV-2 Antigen Rapid Test Kit

SARS-CoV-2 Antigen Rapid Test Kit



  • Results in 15 minutes.
  • 98.5% Accuracy.
  • Highly accurate.
  • Tested and approved.
  • Cost effective solution.
  • Royal Mail Tracked24 Delivery.
  • Detects Active COVID-19 Infection.
  • Detects multiple strains, including the DELTA and Omicron variant.
  • Detects new strains.

For bulk orders please contact us.


SKU: ATGR-PACK Category:
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The Antigen Rapid Test Kit is an immunochromatographic assay for rapid, qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal (NP) and nasal (NS) swab specimens directly or after the swabs have been added to viral transport media from individuals who are suspected of COVID-19.

This test is authorised for use at the Point of Care (POC), i.e., in patient care settings operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation.

Positive results do not rule out bacterial infection or co-infection with other viruses. Negative results should be treated as presumptive, do not rule out SARS-CoV-2 infection and should not be used as the sole basis for treatment or patient management decisions.

Why buy from us?

  • Unique QR code on each test cassette.
  • CE Marked, FDA authorized under a EUA Lateral Flow Antigen test kit.
  • Nasal Specimen sample.
  • Easy to operate.
  • All required accessories are provided in the test kit.
  • Simple to use and fast results.
  • For ages 2 to adult.


Store at room temperature between 2-30°C.


Positive result: Both the “T” position and Control “C” position appear visible colour lines. If the “T” test shows a faint colour, the result is also positive.

Negative result: Only the Control “C” position appears colour, while the test “T” position is blank.

Invalid Result: If the control “C” position and Control “T” position remain blank, the result is invalid because the detecting function is failed to work and retest is required.

Material provided

  • Cassettes.
  • Individually wrapped specimen sampling sterile swab.
  • Extraction tubes.
  • Nozzle for extraction tubes.
  • Bottle of sample extraction buffer.
  • Instruction for use.

Performance Characteristics

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.

Additional information

Weight 2.00 kg
Dimensions 45 × 35 × 16 cm

25 Tests, 50 Tests, 100 Tests


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