The COVID-19/Influenza A+B Antigen Combo Rapid Test Cassette Yodziyesa Tokha (Kugwiritsa Ntchito Kunyumba)Hong KangKulembetsa kwa MDDHKMD No. 230344

Kupangidwa ndi Hangzhou HEO Technology Co., Ltd.

Bungwe la Medical Device Division (MDD), lomwe poyamba linkadziwika kuti Medical Device Control Office (MDCO) MDD ili ndi udindo wokhazikitsa Medical Device Administrative Control System (MDACS) ndikupanga ndondomeko yoyendetsera zipangizo zachipatala kwa nthawi yaitali.Cholinga cha lamuloli ndikuwonetsetsa kuti anthu ku Hong Kong ali ndi mwayi wopeza zida zamankhwala munthawi yake zomwe zili zotetezeka, zogwira mtima, komanso zomwe zimagwira ntchito kumbali imodzi, ndikupewa zolemetsa zosafunikira pamalonda ena.

Zogulitsa zathu, zomwe zadutsa satifiketi yamayiko ena ambiri ndipo zagulitsa bwino kwambiri ndipo tsopano zatsimikiziridwa ndi bungwe la boma, zitha kuyesa kachilombo ka COVID-19 & Influenza A+B bwino kwambiri.

Onani tsamba la satifiketi ya MDD: https://www.mdd.gov.hk/en/whats-new/rapid-antigen-tests-covid-19/index.html

Onani tsamba la satifiketi ya TGA: https://www.tga.gov.au/products/covid-19/covid-19-tests/covid-19-rapid-antigen-self-tests-home-use/covid-19-rapid -antigen-self-mayesero-avomerezedwa-australia