▲ Izifo Zokuphefumula
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HWTS-RT065A/B/C/D-COVID-19 /Flu A &B/ RSV/ADV Ag Ag Combo Rapid Test
Le khithi ihloselwe ukuthola ama-antigen e-SARS-CoV-2, igciwane lomkhuhlane A no-B, igciwane lokuphefumula elihambisana nokuxhumana, kanye ne-Adenovirus kumasampula okuhlolwa kwamakhala okuvela kubantu abasolwa ngokutheleleka zingakapheli izinsuku eziyi-7 kusukela ekuqaleni kwezimpawu kanye nokuxhumana okuseduze ekuxilongweni okuhlukile kokutheleleka kwendlela yokuphefumula yi-SARS-CoV-2, igciwane lomkhuhlane A no-B, igciwane lokuphefumula elihambisana nokuxhumana, kanye ne-Adenovirus. Imiphumela yokuhlolwa akufanele isetshenziswe njengesisekelo sodwa sesinqumo somtholampilo sokuxilongwa nokwelashwa. Ukuxilongwa okwengeziwe kwezokwelapha kufanele kuqinisekiswe ngezindlela zokuhlola ezihlukile kanye neminye imiphumela yezokwelapha. Le khithi ingeyokusetshenziswa kokuxilonga okusebenzisana nokuxhumana kuphela futhi ayizenzakalelayo.
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Ukuhlolwa Okusheshayo kwe-HWTS-RT200A/B/C/D-COVID-19/ Flu A&B Ag
Le khithi ihloselwe ukuthola ama-antigen e-SARS-CoV-2, igciwane lomkhuhlane A kanye no-B ngaphakathi kwe-vitro ngamasampula e-swabs yamakhala avela kubasolwa ngokutheleleka zingakapheli izinsuku eziyi-7 kusukela kuqale izimpawu kanye nokuxhumana okuseduze ekuxilongweni okuhlukile kokutheleleka kwendlela yokuphefumula yi-SARS-CoV-2, igciwane lomkhuhlane A kanye no-B. Imiphumela yokuhlolwa akufanele isetshenziswe njengesisekelo sodwa sesinqumo somtholampilo sokuxilongwa kanye nokwelashwa. Ukuxilongwa okwengeziwe kwezokwelapha kufanele kuqinisekiswe ngezindlela zokuhlola ezihlukile kanye neminye imiphumela yezokwelapha. Le khithi ingeyokuxilongwa kwe-in vitro kuphela futhi ayizenzakalelayo.
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HWTS-RT201A/B/C/D-RSV/ADV Ag Ukuhlolwa Okusheshayo
Le khithi yenzelwe ukuthola ama-antigen e-Respiratory Syncytial Virus kanye ne-Adenovirus ngaphakathi kwe-vitro ngamasampula e-nasal swabs avela kubasolwa ngokutheleleka zingakapheli izinsuku eziyi-7 kusukela izimpawu ziqalile kanye nokuxhumana okuseduze ekuxilongweni okuhlukile kokutheleleka kwendlela yokuphefumula yi-Respiratory Syncytial Virus kanye ne-Adenovirus. Imiphumela yokuhlolwa akufanele isetshenziswe njengesisekelo sodwa sesinqumo somtholampilo sokuxilongwa nokwelashwa. Ukuxilongwa okwengeziwe kwezokwelapha kufanele kuqinisekiswe ngezindlela zokuhlola ezihlukile kanye neminye imiphumela yezokwelapha.
Ikhithi yayiwukuhlolwa kwe-in vitro kuphela futhi ayizenzakalelayo.
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I-Human Metapneumovirus Antigen
Le khithi isetshenziselwa ukuthola ama-antigen e-metapneumovirus omuntu kumasampula e-oropharyngeal swab, ama-nasal swab, kanye namasampula e-nasopharyngeal swab.
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I-SARS-CoV-2, i-Influenza A&B Antigen, i-Respiratory Syncytium, i-Adenovirus kanye ne-Mycoplasma Pneumoniae kuhlangene
Le khithi isetshenziselwa ukuthola i-SARS-CoV-2, i-influenza A&B antigen, i-Respiratory Syncytium, i-adenovirus kanye ne-mycoplasma pneumoniae kumasampula e-nasopharyngeal swab、oropharyngeal swab kanye ne-nasal swab in vitro, futhi ingasetshenziswa ekuxilongeni okuhlukile kokutheleleka okusha kwe-coronavirus, ukutheleleka kwegciwane lokuphefumula le-syncytial, i-adenovirus, i-mycoplasma pneumoniae kanye nokutheleleka kwegciwane le-influenza A noma B. Imiphumela yokuhlolwa ingeyereferensi yomtholampilo kuphela, futhi ayikwazi ukusetshenziswa njengesisekelo sokuxilongwa nokwelashwa kuphela.
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I-SARS-CoV-2, i-Respiratory Syncytium, kanye ne-Influenza A&B Antigen Combined
Le khithi isetshenziselwa ukuthola i-SARS-CoV-2, igciwane lokuphefumula elihambisana nokuxhumana kanye nama-antigen e-influenza A&B in vitro, futhi ingasetshenziswa ekuxilongeni okuhlukile kokutheleleka kwe-SARS-CoV-2, ukutheleleka kwegciwane lokuphefumula elihambisana nokuxhumana, kanye nokutheleleka kwegciwane le-influenza A noma B[1]. Imiphumela yokuhlolwa ingeyereferensi yomtholampilo kuphela futhi ayikwazi ukusetshenziswa njengesisekelo sokuxilongwa nokwelashwa kuphela.
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Ikhithi Yokuthola I-Influenza A Virus H5N1 Nucleic Acid
Le khithi ifaneleka ekutholakaleni kwe-H5N1 nucleic acid yegciwane le-influenza A kumasampula e-nasopharyngeal swab yomuntu ngaphandle kokusebenzisa i-vitro.
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I-Influenza A/B Antigen
Le khithi isetshenziselwa ukuthola ama-antigen e-influenza A kanye ne-B kumasampula e-oropharyngeal swab kanye ne-nasopharyngeal swab.
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I-Adenovirus Antigen
Le khithi yenzelwe ukuthola i-antigen ye-Adenovirus (Adv) esezingeni eliphezulu ngaphakathi kwe-vitro kuma-swabs e-oropharyngeal kanye nama-swabs e-nasopharyngeal.
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I-Antigen Yegciwane Lokuphefumula Elihambisana Nokuphefumula
Le khithi isetshenziselwa ukuthola ama-antigen e-respiratory syncytial virus (RSV) fusion protein kumasampula e-nasopharyngeal noma oropharyngeal swab avela ezinganeni ezisanda kuzalwa noma ezinganeni ezingaphansi kweminyaka emi-5 ubudala.
