Iyo COVID-19/Influenza A+B Antigen Combo Rapid Test Cassette yekuzviongorora (Kushandisa Kumba)Hong KangMDD RegisterHKMD Nhamba 230344

Yakagadzirwa neHangzhou HEO Technology Co., Ltd.

The Medical Device Division (MDD), yaimbozivikanwa seMedical Device Control Office (MDCO) MDD ine basa rekushandisa Medical Device Administrative Control System (MDACS) uye kugadzira hurongwa hwenguva refu hwemitemo yezvishandiso zvekurapa.Chinangwa chemutemo ndechekuona kuti vanhu muHong Kong vawana nguva yekuwana michina yekurapa yakachengeteka, inoshanda, uye inoita sezvakarongwa kune rumwe rutivi, uye kudzivirira mutoro usingakoshi pane kutengeserana kune rimwe divi.

Zvigadzirwa zvedu, izvo zvakapfuura dzimwe nyika dzakawanda chitupa uye zvakatengesa zvakanyanya uye zvino zvakasimbiswa nesangano rehurumende rakadaro, zvinogona kuyedza hutachiona hweCOVID-19 & Influenza A + B zvakanyanya.

Tarisa webhusaiti yechitupa cheMDD: https://www.mdd.gov.hk/en/whats-new/rapid-antigen-tests-covid-19/index.html

Tarisa webhusaiti yechitupa cheTGA: 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-inotenderwa-australia