Ikhithi ye-Antigen yakwa-SARS-CoV-2

  • SARS-CoV-2 Antigen Rapid Test(nasal)

    I-SARS-CoV-2 Antigen Rapid Test (amakhala)

    REF 500200 Ukucaciswa 1 Izivivinyo/Ibhokisi ;5 Izivivinyo/ibhokisi; 20 Izivivinyo/ibhokisi
    Umgomo wokutholwa Ukuhlolwa kwe-Immunochromatographic Izibonelo I-Anterior nasal swab
    Ukusetshenziswa Okuhlosiwe I-StrongStep® SARS-CoV-2 Antigen Rapid Test Cassette isebenzisa ubuchwepheshe be-immunochromatography ukuze ithole i-SARS- CoV-2 nucleocapsid antigen esibonelweni se-swab yamakhala yomuntu yangaphambili.Lokhu testis ukusetshenziswa kanye kuphela futhi ihloselwe ukuzihlola wena.Kunconywa ukuthi usebenzise lesi sivivinyo phakathi nezinsuku ezi-5 zokuqala kwezimpawu.Isekelwa ukuhlolwa kokusebenza komtholampilo.

     

  • SARS-CoV-2 Antigen Rapid Test(Professional Use)

    I-SARS-CoV-2 Antigen Rapid Test (Ukusetshenziswa Okuyingcweti)

    REF 500200 Ukucaciswa 25 Izivivinyo/ibhokisi
    Umgomo wokutholwa Ukuhlolwa kwe-Immunochromatographic Izibonelo I-Anterior nasal swab
    Ukusetshenziswa Okuhlosiwe I-StrongStep® SARS-CoV-2 Antigen Rapid Test Cassette isebenzisa ubuchwepheshe be-immunochromatography ukuze ithole i-SARS- CoV-2 nucleocapsid antigen esibonelweni se-swab yamakhala yomuntu yangaphambili.Lokhu testis ukusetshenziswa kanye kuphela futhi ihloselwe ukuzihlola wena.Kunconywa ukuthi usebenzise lesi sivivinyo phakathi nezinsuku ezi-5 zokuqala kwezimpawu.Isekelwa ukuhlolwa kokusebenza komtholampilo.
  • SARS-CoV-2 Antigen Rapid Test for Saliva

    I-SARS-CoV-2 Antigen Rapid Test yamathe

    REF 500230 Ukucaciswa 20 Izivivinyo/Ibhokisi
    Umgomo wokutholwa Ukuhlolwa kwe-Immunochromatographic Izibonelo
    Amathe
    Ukusetshenziswa Okuhlosiwe Lokhu ukuhlola okusheshayo kwe-immunochromatographic ukuze kutholwe igciwane le-SARS-CoV-2 i-Nucleocapsid Protein antigen ku-swab yamathe womuntu eqoqwe kubantu okusolwa ukuthi bane-COVID-19 ngumhlinzeki wabo wezempilo phakathi kwezinsuku ezinhlanu zokuqala kwezimpawu.I-assay isetshenziswa njengosizo ekuxilongweni kwe-COVID-19.
  • System Device for SARS-CoV-2 & Influenza A/B Combo Antigen Rapid Test

    Idivayisi Yesistimu ye-SARS-CoV-2 & Influenza A/B Combo Antigen Rapid Test

    REF 500220 Ukucaciswa 20 Izivivinyo/Ibhokisi
    Umgomo wokutholwa Ukuhlolwa kwe-Immunochromatographic Izibonelo Amakhala / Oropharyngeal swab
    Ukusetshenziswa Okuhlosiwe Lokhu ukuhlola okusheshayo kwe-immunochromatographic ukuze kutholwe igciwane le-SARS-CoV-2 i-Nucleocapsid Protein antigen ku-human Nasal/Oropharyngeal swab eqoqwe kubantu abasolwa nge-COVID-19 ngumhlinzeki wabo wezempilo phakathi nezinsuku ezinhlanu zokuqala kwezimpawu.I-assay isetshenziswa njengosizo ekuxilongweni kwe-COVID-19.
  • Dual Biosafety System Device for SARS-CoV-2 Antigen Rapid Test

    I-Dual Biosafety System Device ye-SARS-CoV-2 Antigen Rapid Test

    REF 500210 Ukucaciswa 20 Izivivinyo/Ibhokisi
    Umgomo wokutholwa Ukuhlolwa kwe-Immunochromatographic Izibonelo Amakhala / Oropharyngeal swab
    Ukusetshenziswa Okuhlosiwe Lokhu ukuhlola okusheshayo kwe-immunochromatographic kokutholwa kwegciwane le-SARS-CoV-2 i-Nucleocapsid Protein antigen ku-human Nasal / Oropharyngeal swab eqoqwe kubantu abasolwa nge-COVID-19 ngumhlinzeki wabo wezempilo phakathi nezinsuku ezinhlanu zokuqala kwezimpawu.I-assay isetshenziswa njengosizo ekuxilongweni kwe-COVID-19.