Igolide yeColloidal
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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-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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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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Isixhobo sokuchongwa kwe-antibody ye-Chikungunya Virus IgM/IgG (igolide yeColloidal)
[Igama lemveliso]Isixhobo sokuchongwa kwe-antibody ye-Chikungunya Virus IgM/IgG (igolide yeColloidal)
[ImvelisoIkhowudi]I-HWTS-FE062
[Ukusetyenziswa Okucetywayo]
Le khithi yenzelwe ukufumanisa ii-antibodies ezisemgangathweni kwi-vitro
ngokuchasene nentsholongwane yeChikungunya (kuquka i-IgM kunye ne-IgG), kwaye isetyenziswa njengesixhobo sokukhusela
ukuxilongwa okuncedisiweyo kosulelo lwentsholongwane yeChikungunya.
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Amayeza oKhuseleko lwe-Aspirin
Le khithi isetyenziselwa ukufumanisa ubunjani bee-polymorphisms kwiindawo ezintathu zemfuza ze-PEAR1, PTGS1 kunye ne-GPIIIa kwiisampuli zegazi elipheleleyo lomntu.
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Igazi leMilingo yeNdle
Le khithi isetyenziselwa ukufumanisa i-hemoglobin yomntu kwisampuli yendle yomntu ngaphakathi kwi-vitro kunye nokufumanisa ukopha kwangethuba kwamathumbu.
Le khithi ifanelekile ukuba izivavanywe ngabantu abangengoochwephesha, kwaye ingasetyenziswa nabasebenzi bezonyango abaziingcali ukufumanisa igazi kwindle kwiindawo zonyango.
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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-Monkeypox Virus IgM/IgG Antibody
Le khithi isetyenziselwa ukufumanisa ii-antibodies ze-monkeypox virus kwi-in vitro, kuquka i-IgM kunye ne-IgG, kwi-serum yomntu, kwi-plasma nakwisampuli yegazi elipheleleyo.
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I-Hemoglobin kunye neTransferrin
Le khithi isetyenziselwa ukufumanisa ubungakanani obuchanekileyo be-hemoglobin yomntu kunye ne-transferrin kwiisampuli zendle yomntu.
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IiHBsAg kunye neHCV Ab ezidityanisiweyo
Le khithi isetyenziselwa ukufumanisa umgangatho we-antigen yomphezulu we-hepatitis B (HBsAg) okanye i-antibody ye-hepatitis C kwi-serum yomntu, kwi-plasma nakwigazi elipheleleyo, kwaye ifanelekile ukunceda ekuxilongweni kwezigulana ezirhanelwa ukuba zine-HBV okanye i-HCV okanye ukuhlolwa kwamatyala kwiindawo ezinezinga eliphezulu losulelo.
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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.
