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Ikhithi ye-Blood Malaria Pf Antigen Rapid Diagnostic Test
I-Malaria PF Indlela Yokuhlola Okusheshayo: Ulwazi Lokukhiqiza Igolide Le-Colloidal Inombolo Yemodeli Yenombolo ye-MAL-PF Ukupakisha Izivivinyo/ikhithi engama-25, 30kits/CTN Igama Umalaleveva (PF) Ukuhlolwa Okusheshayo Isigaba Isigaba I Izici Ukuzwela Okuphezulu, Isitifiketi sokusebenza okulula CE/ ISO13485 Ukunemba > 99% Shelf Impilo Yeminyaka Emibili Indlela Yokusebenzisa Igolide Isevisi ye-Colloidal OEM/ODM Inqubo Yokuhlola Etholakalayo Funda imiyalelo ozoyisebenzisa ngaphambi kokuhlolwa bese ubuyisela isisebenzi kuzinga lokushisa elilingana negumbi ngaphambi kokuhlolwa.... -
Uhlobo lwegazi kanye nekhithi yokuhlola inhlanganisela Ethathelwanayo
Uhlobo lwegazi kanye nekhithi yokuhlola ye-Infectious Combo Isigaba Esiqinile/I-Colloidal Gold Production Ulwazi Model Number ABO&Rhd/HIV/HBV/HCV/TP-AB Packing 20 Tests/ kit, 30kits/CTN Igama Uhlobo lwegazi Kanye ne-Infectious Combo Test kit Ukuhlukaniswa kwensimbi Isigaba III Izici Eziphakeme ukuzwela, Isitifiketi sokusebenza okulula CE/ ISO13485 Ukunemba > 99% Impilo yeshelufu Iminyaka Emibili Indlela Yokusebenza Isigaba Esiqinile/Isevisi yegolide ye-Colloidal OEM/ODM Inqubo yokuhlola etholakalayo 1 Funda imiyalelo... -
I-xiamen wiz I-CFDA Factory inikeza ukuhlolwa okusheshayo kwe-calprotectin cal
Ikhithi Yokuxilonga yeCalprotectin (Cal) iyigolide elicijile le-semiquantitative ye-cal evela ku-Human Faeces, enenani elibalulekile lokuxilonga lesifo samathumbu esivuvukalayo.I-Carcino-embryonic Antigen
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Ikhithi yokuxilonga i-Helicobacter Pylori Antibody Hp-ab test kit
Le khithi ifanele ukutholwa kwekhwalithi ye-antibody ku-anti-gastric Helicobacter pylori (HP) okungenzeka ukuthi ikhona egazini lomuntu lonke, i-serum noma amasampula e-plasma e-vitro.Ukuze kuhlolwe ezikhungweni zezokwelapha nezempilo, esetshenziswa njenge-axiliary diagnostic reagent ye-gastric helicobacter pylori ukutheleleka ekuxilongweni komtholampilo.
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ukuhlolwa kwasekhaya isinyathelo esisodwa I-Rotavirus Group A test kit latex RV test IVD reagent
Ikhithi yokuxilonga ye-Antigen kuya ku-Rotavirus Group A (i-Latex) ilungele ukutholwa kwekhwalithi ye-antigen ye-Rotavirus Group A kumasampula omswane womuntu.Lokhu kuhlolwa kuhloselwe ukusetshenziswa ngochwepheshe bezempilo kuphela.Phakathi naleso sikhathi, lokhu kuhlolwa kusetshenziselwa ukuxilongwa okuyisizayo kokutheleleka kwe-rotavirus yeqembu A ezigulini ezinohudo olusemtholampilo lwezingane.
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I-antibody ye-IgM kuya kukhithi yokuhlola ye-mycoplasma pneumoniae colloidal gold
Ikhithi Yokuxilonga Ye-IgM Antibody kuya ku-Mycoplasma Pneumoniae iyi-colloidal gold immunochromatographic assay yokunqunywa kwekhwalithi ye-IgM Antibody kuya ku-Mycoplasma Pneumoniae egazini lomuntu lonke, i-serum noma i-plasma, isebenza njenge-Mycoplasma pneumonia infection ekuxilongweni komtholampilo.Okwamanje iyi-reagent yokuhlola.
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Ikhithi yokuhlola ye-cpn igm ikhithi yokuhlola ye-chlamydia pneumoniae igolide elicijile
I-Diagnostic Kit (i-Colloidal Gold) ye-antibody ye-IgM ku-Chlamydia Pneumoniae iyi-colloidal yegolide ye-immunochromatographic assay yokunqunywa kwekhwalithi ye-IgM Antibody kuya ku-Chlamydia Pneumoniae (Cpn-IgM) egazini lomuntu lonke, i-serum noma i-plasma auxilidia yokutheleleka, isebenza njenge-plasma auxilidia i-reagent ekuxilongweni komtholampilo.Okwamanje iyi-reagent yokuhlola.Wonke amasampula amahle kufanele aqinisekiswe ngezinye izindlela.Lokhu kuhlolwa kuhloselwe ukusetshenziswa ngochwepheshe bezempilo kuphela.
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Ikhithi yokuhlola ye-FOB ye-fecal yokuhlolwa kwegazi okukusebenzelayo okulumbayo I-Rapid Test Strips FOB ishidi elingasikiwe
Le khithi ifanele ukutholwa kwekhwalithi ye-antibody ku-anti-gastric Helicobacter pylori (HP) okungenzeka ukuthi ikhona egazini lomuntu lonke, i-serum noma amasampula e-plasma e-vitro.Ukuze kuhlolwe ezikhungweni zezokwelapha nezempilo, esetshenziswa njenge-axiliary diagnostic reagent ye-gastric helicobacter pylori ukutheleleka ekuxilongweni komtholampilo.
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i-colloidal gold adenovirus one step av test kit AV ukuhlolwa okusheshayo kweKid
I-Diagnostic Kit (LATEX) ye-Rotavirus Group A kanye ne-adenovirus ifanele ukutholwa kwekhwalithi ye-Rotavirus Group A kanye ne-adenovirus antigen kumasampula endle yomuntu.Lokhu kuhlolwa kuhloselwe ukusetshenziswa ngochwepheshe bezempilo kuphela.Phakathi naleso sikhathi, lokhu kuhlola kusetshenziselwa ukuhlonza izifo zohudo lwezingane ezigulini ezine-Rotavirus Group A i-rotavirus kanye nokutheleleka kwe-adenovirus.
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Isinyathelo esisodwa esisheshayo sekhithi ye-rotavirus Group kanye ne-Adenovirus latex
I-Diagnostic Kit (LATEX) ye-Rotavirus Group A kanye ne-adenovirus ifanele ukutholwa kwekhwalithi ye-Rotavirus Group A kanye ne-adenovirus antigen kumasampula endle yomuntu.Lokhu kuhlolwa kuhloselwe ukusetshenziswa ngochwepheshe bezempilo kuphela.Phakathi naleso sikhathi, lokhu kuhlola kusetshenziselwa ukuhlonza izifo zohudo lwezingane ezigulini ezine-Rotavirus Group A i-rotavirus kanye nokutheleleka kwe-adenovirus.
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Ikhithi yokuxilonga yeCardiac Troponin I (Fluorescence Immuno Assay)
Ikhithi yokuxilonga ye-Cardiac Troponin I(fluorescence immunochromatographic assay) iwukuhlolwa kwe-fluorescence immunochromatographic ukuze kutholwe inani le-Cardiac Troponin I (cTnI) ku-serum yomuntu noma ku-plasma, isetshenziselwa ukuxilongwa kwe-AMI(Acute Myocardial Infar).
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I-antibody ye-IgM Enterovirus 71 EV71 ikhithi yokuhlola esheshayo EV 71 antibody
I-Diagnostic Kit (i-Colloidal Gold) ye-IgM Antibody to Human Enterovirus 71 iyi-colloidal gold immunochromatographic assay yokunquma ikhwalithi ye-IgM Antibody to Human Enterovirus 71(EV71-IgM) egazini lomuntu lonke, i-serum noma i-plasma.Lokhu kuhlola kuyi-reagent yokuhlola.Wonke amasampula amahle kufanele aqinisekiswe ngezinye izindlela.Lokhu kuhlolwa kuhloselwe ukusetshenziswa ngochwepheshe bezempilo kuphela.
