Iimveliso
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Ikhithi yokuFumanisa utshintsho lwe-EGFR Gene 29 yabantu (i-Fluorescence PCR)-RUO
[Ikhowudi yeMveliso] HWTS- TM4008
Inkcazo emfutshane
Le khithi yenzelwe ukusetyenziswa kuPhando kuphela (i-RUO) kwaye isetyenziselwa ukufumanisa utshintsho oluqhelekileyo kwi-exons 18–21 ye-EGFR gene kwiisampuli ze-DNA ezikhutshiweyo kwizicelo zophando.
Ukusetyenziswa koPhando Kuphela
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Isixhobo sokubona i-Dengue Virus I/II/III/IV eyomileyo ngokuqandisa (Fluorescence PCR)-RUO
[Ikhowudi yeMveliso] HWTS-FE4040
Inkcazo emfutshane
Le khithi isetyenziselwa ukuchonga i-denguevirus (DENV) nucleic acid kwisampuli yeserum yesigulana esikrokrelwayo ukunceda ekuxilongeni izigulana ezineDengue fever. Iziphumo zovavanyo ezifunyenwe yikhithi zezereferensi yeklinikhi kuphela. Ukuze kwenziwe uxilongo lokugqibela, uhlalutyo olupheleleyo lwemeko yesigulana kufuneka lwenziwe kunye neempawu zeklinikhi zesigulana kunye nezinye iziphumo zelebhu.
Ukusetyenziswa koPhando Kuphela
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Iintlobo ezili-18 ze-Human Papilloma Virus enobungozi obuphezulu (16/18 Typing) I-Nucleic Acid Detection Kit (i-Fluorescence PCR)
Ikhowudi yeMveliso
I-HWTS-CC018B
Ukuvunywa kweMveliso
CE, TFDA
Ukusetyenziswa Okucetywayo
Le khithi ifanelekile ekufumaneni iintlobo ezili-18 ze-human papilloma virus (HPV) (HPV16, 18, 26, 31, 33, 35, 39, 45, 51, 52, 53, 56, 58, 59, 66, 68, 73, 82) ze-nucleic acid fragments kwiisampuli zomchamo womntu, iisampuli ze-cervical swab yabasetyhini, iisampuli ze-vaginal swab yabasetyhini kunye ne-HPV 16/18 typing.
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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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Ikhithi yokuFumana ubungakanani be-Human BCR-ABL1 Fusion Gene (i-Fluorescence PCR)-RUO
Le khithi isetyenziselwa ukufumanisa ubungakanani bamanqanaba e-RNA yohlobo lwe-M, uhlobo lwe-m, kunye ne-μ yohlobo lwe-BCR-ABL1 kwiisampuli zophando lwethambo lomntu kunye negazi elipheleleyo kwizicelo zophando. Le mveliso yenzelwe ukusetyenziswa kuphando kuphela (RUO) kwaye ayijoliswanga ekuxilongweni kwezonyango okanye nakweyiphi na enye izicelo zokuxilonga.
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I-KRAS 8 Mutations Detection Kit (Fluorescence PCR)-RUO
[Ikhowudi yeMveliso] HWTS-TM4009
Inkcazo emfutshane
Le khithi yenzelwe ukufumanisa utshintsho olukwi-vitro kwiinguqu ezisi-8 kwi-codons 12 kunye ne-13 ze-K-ras gene kwi-DNA ekhutshiweyo kwiindawo ze-pathological ezifakwe kwi-paraffin yomntu.
Ukusetyenziswa koPhando Kuphela
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Iintlobo ezilithoba zeKit yokuFumanisa i-Nucleic Acid Detection Kit (Fluorescence PCR)
[Igama lemveliso]Iintlobo ezilithoba zeKit yokuFumanisa i-Nucleic Acid yosulelo lweSifo seNtlalo
(I-PCR yeFluorescence)
[ImvelisoIkhowudi]I-HWTS-UR048
[Ukusetyenziswa Okucetywayo]
Le khithi ifanelekile ekufumaneni i-Chlamydia trachomatis (CT) ngendlela esemgangathweni kwi-vitro,Neisseria gonorrhoeae (NG), Mycoplasma hominis (Mh), Herpes Simplex Virus Type1 (HSV1), Ureaplasma urealyticum, UU), Uhlobo lweNtsholongwane yeHerpes Simplex 2 (HSV2),Ureaplasma Parvum (UP), Mycoplasma genitalium (Mg), Trichomonal vaginitis (TV)kumchamo, i-urethral swab yamadoda, i-cervical swab yabasetyhini, kunye neesampuli ze-vaginal swab yabasetyhini,ukubonelela ngoncedo ekuxilongweni nasekunyangweni kwezigulane ezine-genitourinary tractusulelo.
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Iintlobo ezili-17 zeHuman Papillomavirus (16/18/6/11/44 Typing) I-Nucleic Acid Detection Kit (Fluorescence PCR) - Ukusetyenziswa koPhando kuphela
Le khithi ifanelekile ekufumaneni iintlobo ezili-17 ze-human papillomavirus (HPV 6, 11, 16, 18, 31, 33, 35, 39, 44, 45, 51, 52, 56, 58, 59, 66, 68) ze-nucleic acid fragments kwisampuli yomchamo, isampuli ye-cervical swab yabasetyhini kunye nesampuli ye-vaginal swab yabasetyhini, kunye nokufunyanwa kwe-HPV 16/18/6/11/44 typing detection.
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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 kweNucleic Acid yeBundybugyo Virus Ebola (iFluorescence PCR)
[Igama lemveliso] Isixhobo sokuchongwa kweNucleic Acid yeBundybugyo Virus Ebola (iFluorescence PCR)
[ImvelisoIkhowudi] I-HWTS-FE4023
[Inkcazo emfutshane]
Le mveliso yenzelwe ukufumanisa i-nucleic acid kwi-in vitro qualitative qualitative
Intsholongwane ye-Bundybugyo Ebola egazini lomntu lilonke, i-serum/plasma, kunye neesampuli ze-Oral swab.
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Ikhithi yokuFumanisa i-Human Leukocyte Antigen B27 Nucleic Acid (Fluorescence PCR)-RUO
Ikhithi yokuFumanisa i-Human Leukocyte Antigen B27 Nucleic Acid (i-Fluorescence PCR)
I-HWTS-GE011A
Le khithi isetyenziselwa ukufumanisa i-DNA ngokwemigangatho kwiintlobo ze-antigen ze-leukocyte yomntu i-HLA-B*2702, i-HLA-B*2704 kunye ne-HLA-B*2705.
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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.
