Iimveliso
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SARS-CoV-2 & Influenza A/B Multiplex Real-Time PCR Kit
I-REF 510010 Inkcazo Iimvavanyo ezingama-96/Ibhokisi Umgaqo wokufumanisa I-PCR Imizekelo Iimpumlo / i-Nasopharyngeal swab / i-Oropharyngeal swab Usetyenziso olucetywayo IStrongStep® SARS-CoV-2 & Influenza A/B Multiplex Real-Time PCR Kit yenzelwe ukufunyaniswa komgangatho ngaxeshanye kunye nokwahlulwa kwe-SARS-CoV-2, intsholongwane yoMkhuhlane A kunye nentsholongwane ye-Influenza B i-RNA kumnikezeli wezempilo-eqokelelwe ngeempumlo kunye ne-nasopharyngeal swab. okanye iisampulu ze-oropharyngeal swab kunye nesampulu eziqokelelweyo zempumlo okanye i-oropharyngeal swab (eqokelelwe kwindawo yokhathalelo lwempilo ngomyalelo womboneleli wezempilo) kubantu ekurhaneleka ukuba bosulelo lwentsholongwane yokuphefumla oluhambelana ne-COVID-19 ngumboneleli wabo wezempilo.
Ikhithi yenzelwe ukusetyenziswa ngabasebenzi abaqeqeshwe kwilabhoratri
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Vibrio cholerae O1 Antigen Rapid Test
I-REF 501050 Inkcazo Iimvavanyo ezingama-20/Ibhokisi Umgaqo wokufumanisa Uvavanyo lwe-Immunochromatographic Imizekelo Ilindle Usetyenziso olucetywayo I-StrongStep® Vibrio cholerae i-O1 ye-Antigen Rapid Test Device (Iindle) luvavanyo olukhawulezayo olubonakalayo lwe-immunoassay yomgangatho, ukufumanisa okucingelwayo kwe-Vibrio cholerae O1 kwi-fecal specimens zomntu.Le khithi yenzelwe ukusetyenziswa njengoncedo ekuxilongeni usulelo lweVibrio cholerae O1. -
Uvavanyo oluKhawulezayo lwebhaktheriya vaginosis
I-REF 500080 Inkcazo Iimvavanyo ezingama-50 / Ibhokisi Umgaqo wokufumanisa PH ixabiso Imizekelo Ukuphuma kwilungu lobufazi Usetyenziso olucetywayo Inyathelo Eliqinileyo®I-Bacterial vaginosis(BV) Isixhobo soVavanyo oluKhawulezayo sijonge ukulinganisa i-pH yelungu lobufazi ukunceda ekuxilongeni i-Bacterial vaginosis. -
Uvavanyo lweProcalcitonin
I-REF 502050 Inkcazo Iimvavanyo ezingama-20/Ibhokisi Umgaqo wokufumanisa Uvavanyo lwe-Immunochromatographic Imizekelo I-Plasma / iSerum / Igazi elipheleleyo Usetyenziso olucetywayo Inyathelo Eliqinileyo®Uvavanyo lweProcalcitonin luvavanyo olukhawulezayo lwe-immune-chromatographic yokufumanisa i-semi-quantitative ye-Procalcitonin kwiserum yomntu okanye kwiplasma.Isetyenziselwa ukuxilonga kunye nokulawula unyango olunzima, usulelo lwebhaktheriya kunye ne-sepsis. -
Uvavanyo oluKhawulezayo lwe-SARS-CoV-2 IgM/IgG Antibody
I-REF 502090 Inkcazo Iimvavanyo ezingama-20/Ibhokisi Umgaqo wokufumanisa Uvavanyo lwe-Immunochromatographic Imizekelo Igazi elipheleleyo / iSerum / iPlasma Usetyenziso olucetywayo Olu luvavanyo olukhawulezayo lwe-immuno-chromatographic ekubhaqweni ngaxeshanye kwe-IgM kunye ne-IgG antibodies kwi-SARS-CoV-2 intsholongwane egazini lomntu lonke, i-serum okanye iplasma. Uvavanyo lulinganiselwe e-US ukuba lusasazwe kwiilabhoratri eziqinisekiswe yi-CLIA ukwenza uvavanyo olunzima kakhulu.
Olu vavanyo aluzange luhlolwe yi-FDA.
Iziphumo ezibi aziluthinteli usulelo oluqatha lwe-SARS-CoV-2.
Iziphumo zovavanyo lwe-antibody akufuneki zisetyenziselwe ukuxilonga okanye ukungabandakanyi usulelo oluqatha lwe-SARS-CoV-2.
Iziphumo ezincumisayo zisenokuba ngenxa yosulelo lwangaphambili okanye lwangoku lohlobo lwe-coronavirus engeyiyo i-SARS-CoV-2, efana ne-coronavirus HKU1, NL63, OC43, okanye 229E.
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Neisseria gonorrhoeae/Chlamydia trachomatis Antigen Combo Rapid Test
I-REF 500050 Inkcazo Iimvavanyo ezingama-20/Ibhokisi Umgaqo wokufumanisa Uvavanyo lwe-Immunochromatographic Imizekelo Umlomo wesibeleko / urethra swab
Usetyenziso olucetywayo Olu luvavanyo olukhawulezayo lwe-lateral-flow immunoassay ekubhaqweni komgangatho we-Neisseria gonorrhoeae/Chlamydia trachomatis antigens kwi-urethral yamadoda kunye ne-swab yomlomo wesibeleko. -
Uvavanyo olukhawulezayo lwe-Neisseria Gonorrhoeae Antigen Rapid
I-REF 500020 Inkcazo Iimvavanyo ezingama-20/Ibhokisi Umgaqo wokufumanisa Uvavanyo lwe-Immunochromatographic Imizekelo Umlomo wesibeleko / urethra swab Usetyenziso olucetywayo Kufanelekile ukufumanisa ikhwalithi ye-gonorrhoea / i-chlamydia trachomatis antigens kwiimfihlo zomlomo wesibeleko zabasetyhini kunye neesampuli ze-urethral zamadoda kwi-vitro kumaziko ahlukeneyo ezonyango ukuze kuxilongwe ukuxilongwa kwentsholongwane ye-pathogen engentla. -
Isixhobo seCryptococcal Antigen Rapid Test
I-REF 502080 Inkcazo Iimvavanyo ze-20 / Ibhokisi;Iimvavanyo ezingama-50 / Ibhokisi Umgaqo wokufumanisa Uvavanyo lwe-Immunochromatographic Imizekelo Cerebrospinal fluid/Serum Usetyenziso olucetywayo I-StrongStep®Cryptococcal Antigen Rapid Test Device luvavanyo olukhawulezayo lwe-immune-chromatographic lokukhangela i-capsular polysaccharide antigens ye-Cryptococcus species complex (i-Cryptococcus neoformans kunye ne-Cryptococcus gattii) kwi-serum, i-plasma, igazi elipheleleyo kunye ne-cerebral spinal fluid (CSF) -
Candida Albicans Antigen Rapid Test
I-REF 500030 Inkcazo Iimvavanyo ezingama-20/Ibhokisi Umgaqo wokufumanisa Uvavanyo lwe-Immunochromatographic Imizekelo Umlomo wesibeleko / urethra swab Usetyenziso olucetywayo I-StrongStep® Candida albicans Antigen Rapid Test luvavanyo lwe-immunochromatographic olufumanisa ii-antigens ze-pathogen ngokuthe ngqo kwi-swabs ye-vaginal.
