Order COVID-19 Test Kits
Product Features
- Fast and reliable COVID-19 screening
- Results in just 10 minutes allow doctors to make decisions quickly
- Clear and simple to read results
- Easy deployment for large scale testing
- Nasopharyngeal swab specimen
- Kit contains all necessary items and reagents – just add a timer!
Clinical Evidence
Instructions for Use
Specifications
| Sample Type | Nasopharyngeal Swab |
| Equipment Required | Timer |
| Test Time | 10 min |
| Storage Temperature | 2-30°C |
| Operation Temperature | 2-30°C |
| Shelf Life (sealed) | 12 months |
The Novel Coronavirus (SARS-Cov-2) Antigen Rapid Test Cassette (swab) is an in vitro diagnostic test for the qualitative detection of novel coronavirus antigens in Nasopharyngeal swab, using the rapid immunochromatographic method. The identification is based on the monoclonal antibodies specific for the novel coronavirus antigen. The easy to use and rapid point of care application of the test facilitates deployment of large-scale screening in environments where rapid, on-site testing is vital to ensure public health safety.
ALWAYS REFER TO THE INSTRUCTIONS FOR USE – Negative results do not rule out SARS-CoV-2 infection, particularly in those who have been in contact with the virus. Results should not be used as the sole basis to diagnose or exclude SARS-CoV-2 infection or to inform infection status.
COVID-19 IgG/IgM Rapid Screening Test
Product Features
- Accurate results. Fast. 92% accuracy (vs. PCR-confirmed test specimens)
- Results in just 10 minutes allow doctors to make decisions quickly
- Simple finger prick specimen facilitates screening quickly at point-of-care
- Clear and easy to read results
- Easy to use with choice of whole blood, serum or plasma specimen
Clinical Evidence
Instructions for Use
Specifications
| Sample Type | Whole blood, serum or plasma |
| Sample Volume | 2 drops of whole blood (approximately 20 μL) |
| Test Time | 10 min |
| Storage Temperature | 4-30°C |
| Operation Temperature | 4-30°C |
| Shelf Life (sealed) | 12 months |
COVID-19 Global Research Links
S. Lei et al., Clinical characteristics and outcomes of patients undergoing surgeries during the incubation period of COVID-19 infection, EClinicalMedicine (2020), https://doi.org/10.1016/j.eclinm.2020.100331
What is a COVID-19 IgG/IgM Rapid test?
The COVID-19 IgG/IgM Rapid test requires a few drops of blood and is conducted at point-of-care. It detects the presence of IgG and/or IgM antibodies to SARS-CoV2.
Your immune system creates antibodies (complex protein structures) to fight infection. Once you have become exposed to any virus, your body will create different types of immunoglobulins that target that specific virus. These are called IgM (early antibodies, non-specific) and IgG (produced later, and much more specific antibodies).
The COVID-19 IgG/IgM Rapid test detects the presence of your antibodies (IgM and/or IgG) against the COVID-19 virus. It is important to note that your body may not start producing antibodies until several days after initial infection as per the graph below.
IMPORTANT NOTE – The Covid-19 IgG/IgM Rapid Screening Tests are NOT home tests and can only be administered by a registered health professional. More detailed information can be found on the TGA website here https://www.tga.gov.au/legal-supply-covid-19-test-kits.
Under Australian TGA regulations we can only supply testing kits to the following:
- Laboratories that are accredited pathology laboratories
- Medical practitioners who are registered under the law of a State or Territory (this includes commercial companies who have medical professionals employed who can administer the tests)
- Health care professionals in residential and aged care facilities
- Commonwealth, State or Territory department of health
- An agency of the Commonwealth, State or Territory acting on behalf of the Commonwealth, State or Territory department of health.
ALWAYS READ THE INSTRUCTIONS FOR USE: Negative results do not rule out SARS-CoV-2 infection, particularly in those who have been in contact with the virus. Follow-up testing with a molecular diagnostic should be considered to rule out infection in these individuals. Results from antibody testing should not be used as the sole basis to diagnose or exclude SARS-CoV-2 infection or to inform infection status.
Beware of non-TGA approved testing kits. Our COVID-19 IgG/IgM Rapid testing kits are fully TGA approved – ARTG# 334501.
Additional data available on request.
COVID-19 Rapid Test Order Form
To order test kits, please fill in the form below and we will be in contact with you soon.
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Brisbane, Sunshine Coast & Gold Coast, Queensland