The COVID-19/Influenza A+B Antigen Combo Rapid Test Cassette for Self Testing (Home Use)                   Hong Kang MDD Register  HKMD No. 230344

Mufacture by Hangzhou HEO Technology Co., Ltd. 

The Medical Device Division (MDD), formerly known as Medical Device Control Office (MDCO) The MDD is responsible for implementing the Medical Device Administrative Control System (MDACS) and developing a long-term statutory regulatory framework for medical devices. The purpose of regulation is to ensure people in Hong Kong have timely access to medical devices that are safe, efficacious, and perform as intended on one hand, and to avoid unnecessary burden on the trade on the other.

Our products, which has passed many other countries certificate and have sold very well and now is certified by such a government organization, can test the COVID-19 & Influenza A+B virus very well.

Check MDD certificate website : https://www.mdd.gov.hk/en/whats-new/rapid-antigen-tests-covid-19/index.html

Check  TGA certificate website: https://www.tga.gov.au/products/covid-19/covid-19-tests/covid-19-rapid-antigen-self-tests-home-use/covid-19-rapid-antigen-self-tests-are-approved-australia