I-COVID-19

  • 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.
  • Novel Coronavirus (SARS-CoV-2) Multiplex Real-Time PCR Kit

    I-Novel Coronavirus (SARS-CoV-2) Multiplex Real-Time PCR Kit

    REF 500190 Ukucaciswa 96 Izivivinyo/Ibhokisi
    Umgomo wokutholwa I-PCR Izibonelo Ikhala / i-Nasopharyngeal swab
    Ukusetshenziswa Okuhlosiwe Lokhu kuhloswe ukuthi kusetshenziselwe ukuthola ukutholwa kwekhwalithi ye-SARS-CoV-2 yegciwane le-RNA ekhishwe ku-nasopharyngeal swabs, i-oropharyngeal swabs, isikhwehlela kanye ne-BALF ezigulini ngokuhlangana nohlelo lokukhipha i-FDA/CE IVD kanye nezinkundla ezimisiwe ze-PCR ezibalwe ngenhla.

    Ikhithi ihloselwe ukusetshenziswa ngabasebenzi abaqeqeshwe elabhorethri

     

  • SARS-CoV-2 & Influenza A/B Multiplex Real-Time PCR Kit

    I-SARS-CoV-2 & Influenza A/B Multiplex Real-Time PCR Kit

    REF 510010 Ukucaciswa 96 Izivivinyo/Ibhokisi
    Umgomo wokutholwa I-PCR Izibonelo Ikhala / i-Nasopharyngeal swab / i-Oropharyngeal swab
    Ukusetshenziswa Okuhlosiwe

    I-StrongStep® SARS-CoV-2 & Influenza A/B Multiplex Real-Time PCR Kit ihloselwe ukutholwa kwekhwalithi kanye kanye nokuhlukaniswa kwe-SARS-CoV-2, igciwane loMkhuhlane A kanye negciwane le-RNA le-Influenza B kumhlinzeki wezempilo eqoqwe i-swab yamakhala kanye ne-nasopharyngeal. noma izibonelo ze-oropharyngeal swab kanye nezibonelo ze-swab zamakhala noma ze-oropharyngeal oziqoqele zona (eziqoqwe endaweni yokunakekelwa kwezempilo ngokuyalelwa umhlinzeki wezempilo) ezivela kubantu okusolwa ukuthi banegciwane lokuphefumula elihambisana ne-COVID-19 ngumhlinzeki wabo wezempilo.

    Ikhithi ihloselwe ukusetshenziswa ngabasebenzi abaqeqeshwe elabhorethri

     

  • SARS-CoV-2 IgM/IgG Antibody Rapid Test

    Ukuhlolwa Okusheshayo kwe-SARS-CoV-2 IgM/IgG Antibody

    REF 502090 Ukucaciswa 20 Izivivinyo/Ibhokisi
    Umgomo wokutholwa Ukuhlolwa kwe-Immunochromatographic Izibonelo Igazi Eliphelele / I-Serum / Plasma
    Ukusetshenziswa Okuhlosiwe Lokhu ukuhlola okusheshayo kwe-immuno-chromatographic kokutholwa ngasikhathi sinye kwamasosha omzimba e-IgM ne-IgG kugciwane le-SARS-CoV-2 egazini lomuntu lonke, i-serum noma i-plasma.

    Ukuhlola kukhawulelwe e-US ukuthi kusakazwe ezindaweni zokucwaninga ezigunyazwe yi-CLIA ukuze zenze ukuhlola okuyinkimbinkimbi.

    Lokhu kuhlolwa akuzange kubuyekezwe yi-FDA.

    Imiphumela engemihle ayikuvimbeli ukutheleleka okukhulu kwe-SARS-CoV-2.

    Imiphumela yokuhlolwa kwe-antibody akufanele isetshenziselwe ukuxilonga noma ukukhipha ukutheleleka kwe-SARS-CoV-2 okuyingozi.

    Imiphumela emihle ingase ibe ngenxa yokutheleleka kwangaphambilini noma kwamanje ngezinhlobo ze-coronavirus ezingezona ze-SARS-CoV-2, njenge-coronavirus HKU1, NL63, OC43, noma 229E.