I-SARS-CoV-2
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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. -
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. -
I-SARS-CoV-2 Antigen Rapid Test yamathe
REF 500230 Ukucaciswa 20 Izivivinyo/Ibhokisi Umgomo wokutholwa Ukuhlolwa kwe-Immunochromatographic Izibonelo AmatheUkusetshenziswa 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. -
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. -
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. -
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
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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
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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.
