▲ Iintsholongwane zokuphefumla
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HWTS-RT065A/B/C/D-COVID-19 /Flu A &B/ RSV/ADV Ag Combo Rapid Test
Le khithi yenzelwe ukubhaqa ii-antigens ze-SARS-CoV-2, i-Influenza virus A kunye ne-B, i-Respiratory Syncytial Virus, kunye ne-Adenovirus kwisampuli ze-nasal swabs ezivela kubarhanelwa ukuba banentsholongwane zingadlulanga iintsuku ezi-7 emva kokuqala kweempawu kunye nokudibana okusondeleyo ekuxilongweni okwahlukileyo kwentsholongwane yendlela yokuphefumla yi-SARS-CoV-2, i-Influenza Virus A kunye ne-B, i-Respiratory Syncytial Virus, kunye ne-Adenovirus. Iziphumo zovavanyo akufuneki zisetyenziswe njengesiseko sodwa sesigqibo seklinikhi sokuxilonga kunye nonyango. Ukuxilongwa okungakumbi kweklinikhi kufuneka kuqinisekiswe ngeendlela ezahlukeneyo zovavanyo kunye nezinye iziphumo zeklinikhi. Le khithi yenzelwe ukusetyenziswa kwe-in vitro kuphela kwaye ayizenzekeli.
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Uvavanyo olukhawulezileyo lwe-HWTS-RT200A/B/C/D-COVID-19/ Flu A&B Ag
Le khithi yenzelwe ukubona i-antigens ye-SARS-CoV-2, i-Influenza virus A kunye ne-B kwisampuli ze-nasal swabs ezivela kubarhanelwa ukuba banentsholongwane zingadlulanga iintsuku ezi-7 emva kokuqala kweempawu kunye noqhagamshelwano olusondeleyo ekuxilongweni okwahlukileyo kwentsholongwane yendlela yokuphefumla yi-SARS-CoV-2, i-Influenza virus A kunye ne-B. Iziphumo zovavanyo akufuneki zisetyenziswe njengesiseko sodwa sesigqibo seklinikhi sokuxilonga kunye nonyango. Ukuxilongwa okungakumbi kweklinikhi kufuneka kuqinisekiswe ngeendlela ezahlukeneyo zovavanyo kunye nezinye iziphumo zeklinikhi. Le khithi yenzelwe ukuxilongwa kwe-in vitro kuphela kwaye ayizenzekeli.
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HWTS-RT201A/B/C/D-RSV/ADV Ag Rapid Test
Le khithi yenzelwe ukubhaqa i-antigens ye-Respiratory Syncytial Virus kunye ne-Adenovirus kwisampuli ze-nasal swabs ezivela kubantu abarhanelwa ukuba banentsholongwane zingadlulanga iintsuku ezisi-7 emva kokuba iimpawu ziqalile kwaye zisondelelene ekuxilongweni ngokwahlukileyo kwentsholongwane yendlela yokuphefumla yi-Respiratory Syncytial Virus kunye ne-Adenovirus. Iziphumo zovavanyo akufuneki zisetyenziswe njengesiseko sodwa sesigqibo seklinikhi sokuxilonga kunye nonyango. Ukuxilongwa okungakumbi kweklinikhi kufuneka kuqinisekiswe ngeendlela ezahlukeneyo zovavanyo kunye nezinye iziphumo zeklinikhi.
Le khithi yayiyeyokuxilongwa kwi-vitro kuphela kwaye ayizenzekeli.
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I-Human Metapneumovirus Antigen
Le khithi isetyenziselwa ukufumanisa i-antigens ye-metapneumovirus yabantu kwi-oropharyngeal swab, kwi-nasal swabs, nakwiisampuli ze-nasopharyngeal swab.
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I-SARS-CoV-2, i-Influenza A&B Antigen, i-Respiratory Syncytium, i-Adenovirus kunye ne-Mycoplasma Pneumoniae zidityanisiwe
Le khithi isetyenziselwa ukufumanisa i-SARS-CoV-2, i-influenza A&B antigen, i-Respiratory Syncytium, i-adenovirus kunye ne-mycoplasma pneumoniae kwiisampuli ze-nasopharyngeal swab, i-oropharyngeal swab kunye ne-nasal swab kwi-vitro, kwaye ingasetyenziselwa ukuchonga ngokwahlukileyo usulelo olutsha lwe-coronavirus, usulelo lwe-respiratory syncytial virus, i-adenovirus, i-mycoplasma pneumoniae kunye nosulelo lwe-influenza A okanye i-B virus. Iziphumo zovavanyo zezereferensi yeklinikhi kuphela, kwaye azinakusetyenziswa njengesiseko sodwa sokuxilongwa kunye nonyango.
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I-SARS-CoV-2, i-Respiratory Syncytium, kunye ne-Influenza A&B Antigen Combined
Le khithi isetyenziselwa ukufumanisa i-SARS-CoV-2, intsholongwane yokuphefumla kunye ne-influenza A&B antigens in vitro, kwaye ingasetyenziselwa ukufumanisa umahluko phakathi kosulelo lwe-SARS-CoV-2, usulelo lwentsholongwane yokuphefumla kunye ne-influenza syncytial, kunye nosulelo lwentsholongwane ye-influenza A okanye B[1]. Iziphumo zovavanyo zezereferensi yeklinikhi kuphela kwaye azinakusetyenziswa njengesiseko sodwa sokuxilongwa kunye nonyango.
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Ikhithi yokuFumanisa i-Influenza A Virus H5N1 Nucleic Acid
Le khithi ifanelekile ekufumaneni i-influenza A virus H5N1 nucleic acid kwiisampuli ze-human nasopharyngeal swab kwi-vitro.
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I-Influenza A/B Antigen
Le khithi isetyenziselwa ukufumanisa i-antigens ye-influenza A kunye ne-B kwiisampuli ze-oropharyngeal swab kunye ne-nasopharyngeal swab.
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I-Antegen ye-Adenovirus
Le khithi yenzelwe ukufumanisa i-antigen ye-Adenovirus (Adv) kwi-oropharyngeal swabs nakwi-nasopharyngeal swabs kwi-in vitro qualitative.
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I-Antigen yeVirus ehambelanayo yokuphefumla
Le khithi isetyenziselwa ukufumanisa i-antigens ye-respiratory syncytial virus (RSV) fusion protein protein kwiisampuli ze-nasopharyngeal okanye ze-oropharyngeal swab ezivela kwiintsana okanye kubantwana abangaphantsi kweminyaka emi-5 ubudala.
