Covid Rapid Test Pen

Enquiries / Support

0414 338 009 info@ozmedical.com.au

ORDER QUALIFICATION CONSENT

Kits are for authorised medical users only

Based on the below TGA rules on use of the Rapid Antigen Devices, Oz Medical can only sell the rapid antigen device(s) to one or more of the following:

  1. A medical practitioner, or an organisation, business or institution that employs or engages a medical practitioner, registered to practice under a law of a state or territory, where the practitioner is responsible for performing or supervising the performance of the test, and both the practitioner and a person acting under the practitioner’s supervision to perform the test have received training in the correct use of the Device and interpretation of the test result;
  2. A residential care or aged care facility that employs or engages a health practitioner, within the meaning of the Therapeutic Goods Act 1989, where the practitioner is responsible for performing or supervising the performance of the test, and both the practitioner and a person acting under the practitioner’s supervision to perform the test have received training in the correct use of the Device and interpretation of the test result;
  3. An organisation, business or institution that does not have the primary function of providing healthcare services but employs or engages a health practitioner within the meaning of the Therapeutic Goods Act 1989, where the practitioner is responsible for performing or supervising the performance of the test, where both the practitioner and a person acting under the practitioner’s supervision to perform the test have received training in the correct use of the Device and interpretation of the test result;

 I/We meet the TGA rules on use of the Rapid Antigen Devices