I-COVID-19/Influenza A+B Antigen Combo Rapid Test Cassette Yokuzihlola (Ukusetshenziswa Ekhaya)Hong KangIrejista ye-MDDI-HKMD No. 230344

Ikhishwe yi-Hangzhou HEO Technology Co., Ltd.

I-Medical Device Division (MDD), phambilini eyayaziwa ngokuthi i-Medical Device Control Office (MDCO) I-MDD inesibopho sokuqalisa i-Medical Device Administrative Control System (MDACS) kanye nokwakha uhlaka lokulawula olusemthethweni lwesikhathi eside lwemishini yezokwelapha.Inhloso yokulawula iwukuqinisekisa ukuthi abantu base-Hong Kong banokufinyelela ngesikhathi kumishini yezokwelapha ephephile, esebenzayo, futhi esebenza njengoba kuhlosiwe ngakolunye uhlangothi, kanye nokugwema umthwalo ongadingekile kohwebo ngakolunye.

Imikhiqizo yethu, eye yadlula isitifiketi samanye amazwe amaningi futhi ithengiswe kahle kakhulu futhi manje isigunyazwe inhlangano enjalo kahulumeni, ingahlola igciwane le-COVID-19 & Influenza A+B kahle kakhulu.

Hlola iwebhusayithi yesitifiketi se-MDD : https://www.mdd.gov.hk/en/whats-new/rapid-antigen-tests-covid-19/index.html

Bheka iwebhusayithi yesitifiketi se-TGA: https://www.tga.gov.au/products/covid-19/covid-19-tests/covid-19-rapid-antigen-self-tests-home-use/covid-19-rapid -i-antigen-self-test-approved-australia