Ikhithi yovavanyo olukhawulezayo olukhawulezayo lwe-Covid-19 yovavanyo lwe-antigen yempumlo ye-swab

inkcazelo emfutshane:

Iimvavanyo ezingama-20 kwibhokisi enye

OEM yamkelekile

ISO/CE ivunyiwe


  • Ixesha lovavanyo:10-15 imizuzu
  • Ixesha elisebenzayo:Iinyanga ezingama-24
  • Ukuchaneka:Ngaphezulu kwe-99%
  • Inkcazo:1/25 uvavanyo / ibhokisi
  • Ubushushu bokugcina :2℃-30℃
  • Iinkcukacha zeMveliso

    Iithegi zeMveliso

    UKUSETYENZISWA OKUHLOSIWEYO

    I-SARS-CoV-2 i-Antigen Rapid Test (i-Colloidal Gold) yenzelwe ukufunyaniswa komgangatho we-SARS-CoV-2 Antigen (iprotein ye-Nucleocapsid) kwisampulu ze-swab zempumlo kwi-vitro.Iziphumo ezilungileyo zibonisa ubukho be-antigen ye-SARS-CoV-2.Kufuneka ifunyaniswe ngakumbi ngokudibanisa imbali yesigulana kunye nolunye ulwazi loxilongo .Iziphumo ezilungileyo azibandakanyi usulelo lwebhaktheriya okanye olunye usulelo lwentsholongwane.Iintsholongwane ezifunyenweyo azingoyena nobangela uphambili weempawu zesifo.Iziphumo ezibi azilubandakanyi usulelo lwe-SARS-CoV-2, kwaye akufuneki ibe kuphela kwesiseko sonyango okanye izigqibo zolawulo lwezigulane (kubandakanywa nezigqibo zolawulo losulelo).Nika ingqalelo kwimbali yoqhagamshelwano yamva nje yesigulana, imbali yonyango kunye neempawu ezifanayo kunye neempawu ze-COVID-19, ukuba kuyimfuneko, kuyacetyiswa ukuba uqinisekise ezi sampuli ngovavanyo lwe-PCR kulawulo lwesigulana.Yeyabasebenzi baselabhoratri abafumene isikhokelo okanye uqeqesho lobuchwephesha kwaye banolwazi lobuchwephesha lokuxilongwa kwe-in vitro, kunye nabasebenzi abafanelekileyo abafumene ulawulo losulelo okanye uqeqesho lokonga.

    Uvavanyo olukhawulezayo lweAntigen2Uvavanyo olukhawulezayo lwe-Antigen  Wamkelekile kuqhagamshelwano ngeenkcukacha ezithe vetshe!

     


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