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EASY TO USE
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This test does NOT determine if you had COVID-19 in the past or if you have immunity.
Q & A
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ABOUT ANTIGEN
ABOUT ANTIGEN
THE DIFFERENCE BETWEEN A MOLECULAR, ANTIGEN AND ANTIBODY TEST
THE DIFFERENCE BETWEEN A MOLECULAR, ANTIGEN AND ANTIBODY TEST
WILL THIS HURT
WILL THIS HURT
ABOUT ACCURATE
ABOUT ACCURATE
USED ON CHILDREN
USED ON CHILDREN
WILL THIS TEST TELL ME IF I HAVE BEEN INFECTED WITH COVID-19 IN THE PAST
WILL THIS TEST TELL ME IF I HAVE BEEN INFECTED WITH COVID-19 IN THE PAST
ABOUT EXPIRATION DATE
ABOUT EXPIRATION DATE
ABOUT THE SWAB
ABOUT THE SWAB
ABOUT PREGNANCT
ABOUT PREGNANCT
ABOUT THE NEW VARIANTS
ABOUT THE NEW VARIANTS
CAN THIS TEST BE USED MORE THAN ONCE
CAN THIS TEST BE USED MORE THAN ONCE
HOW TO DISPOSE OF A USED TEST
HOW TO DISPOSE OF A USED TEST
ABOUT POSITIVE RESULT
ABOUT POSITIVE RESULT
ABOUT NEGATIVE RESULT
ABOUT NEGATIVE RESULT
ABOUT INVALID RESULT
ABOUT INVALID RESULT
POSSIBLE RISK
POSSIBLE RISK
Antigens are proteins that are part of the COVID-19 virus. If the test detects antigens in your swab sample, it means that the COVID-19 virus is present in your body.
There are three main types of COVID-19 tests. Molecular tests detect the genetic material of the coronavirus. The WonderMED™ COVID-19 Antigen Self-Test is an antigen test. Antigen tests detects coronavirus proteins. Both molecular and antigen tests can tell you if you have an active infection. Antibody tests detect antibodies produced by your body‘s immune system in response to a previous COVID-19 infection. Antibody tests cannot be used to diagnose an active COVID-19 infection.
When the foam end of the swab is inserted in your nose, the nasal swab is not sharp and it should not hurt. Sometimes the swab can feel slightly uncomfortable or tickly. If you feel pain, stop the test and seek advice from a healthcare provider.
Independent evaluation has been conducted by BIOMEX (July 2021).
402 people were evaluated (102 symptomatic within 7 days of onset; 300 asymptomatic).
Results show a very high level of test accuracy - 99.5%, 95% CI (98.20-99.86%).
Suitable for people aged 16 and over using independently. Children under 16 need use under supervision. Keep the test kits away from young children to reduce the risk of accidentally drinking the buffer liquid or swallowing small parts.
DO NOT USE on anyone under 2 years of age
No, this is an antigen test that only detects an active infection. Antibody tests can detect past infections.
The test has an expiration date printed on the box, and should not be used after that date.
DO NOT use anyother swabs! Only use the components included in the test kit.
Pregnancy had no impact on the performance of the test
Variants can be detected. The list of variants of COVID-19 the test can detect (eg. alpha, beta, delta,etc.)
No – each test can only be used once.
Place the swab, tube, and test device into the disposal bag. Seal the bag tightly. Throw away the bag in a waste bin.
A positive result means it is very likely you have SARS-CoV-2 infection. Please isolate yourself, stay at home, avoid contact with your roommates as much as possible and don't receive visitors. Contact your doctor or call the Corona hotline. A positive test result must be confirmed by a LABORATORY PCR test.
This means you probably don't have SARS-CoV-2 infection. Pay attention! A negative result of a self-test is not 100% reliable. So stay careful. You still need to take precautions. Keep your distance, wear a mouth mask and wash your hands often.
An invalid result means this test was unable to determine whether you have SARS-CoV-2 or not. A new test is needed to
get a valid result.
Slight discomfort during the nasal sample collection.
Possible false test results may occur, if symptoms continue, you should repeat the test after 1-2 days, as the coronavirus may not be detectable in the very early phases of infection. You are also advised to continue following local guidelines for self-isolation and consult your doctor.
Customer Care
9am-8pm/7 1300009224 |
To report performance or usability issues contact either WonderMED Technical Support on the number above or the Therapeutic Goods Administration (TGA) via the Users Medical Device Incident Report or by emailing iris@tga.gov.au or calling 1800 809 361.

Notice under section 9D of the Therapeutic Goods Act 1989 of decision to vary ARTG inclusions for medical devices. ARTG coming soon.
GMDN Code and Term Severe acute respiratory syndrome-associated coronavirus IVDs [CT772] Class 3
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