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KaiBiLi COVID-19 IgG/IgM Featured Image
  • KaiBiLi COVID-19 IgG/IgM
  • KaiBiLi COVID-19 IgG/IgM

I-KaiBiLi COVID-19 IgG/IgM

Isitifiketi se-CE

I-KaiBiLiTMI-COVID-19 IgG/IgM Rapid Test Device iyi-lateral flow chromatographic immunoassay yokutholwa kwekhwalithi yamasosha omzimba e-IgG kanye ne-IgM ku-2019-Novel Coronavirus egazini lomuntu lonke, i-serum noma isampula se-plasma.


Imininingwane Yomkhiqizo

Isingeniso

I-KaiBiLiTMI-COVID-19 IgG/IgM Rapid Test Device iyi-lateral flow chromatographic immunoassay yokutholwa kwekhwalithi yamasosha omzimba e-IgG kanye ne-IgM ukuya ku-2019- Novel Coronavirus egazini lomuntu lonke, i-serum noma isampula se-plasma.Isetshenziswa kuphela njengenkomba eyengeziwe yokuthola amacala amasha asolwayo okutholwa kwe-coronavirus nucleic acid engalungile noma ngokuhlangana nokutholwa kwe-nucleic acid ekuxilongweni kwamacala asolwayo.Ngeke isetshenziswe njengesisekelo sokuxilongwa kanye nokukhishwa kwe-pneumonitis etheleleke ngokutheleleka kwe-2019-nCoV.Ayilungele ukuhlolwa kwabantu okuvamile.

Noma yisiphi isifanekiso esisebenzayo esine-COVID-19 IgG/IgM Rapid Test Device kufanele siqinisekiswe ngezinye izindlela zokuhlola kanye nokutholakele emitholampilo.Umphumela wokuhlolwa othi unayo idinga ukuqinisekiswa okwengeziwe.Imiphumela engemihle ayikuvimbeli ukutheleleka okukhulu kwe-2019-nCoV.Uma kusolwa ukutheleleka okuyingozi, ukuhlolwa okuqondile kwe-COVID-19 antigen kuyadingeka.Imiphumela emihle engelona iqiniso ye-COVID-19 IgG/IgM Rapid Test ingase yenzeke ngenxa yokuhlangana kabusha okuvela kumasosha omzimba avele akhona noma ezinye izimbangela ezingaba khona.Ngenxa yengozi yemiphumela emihle engamanga, ukuqinisekiswa kwemiphumela emihle kufanele kucatshangelwe kusetshenziswa ukuhlolwa kwesibili, okuhlukile kwe-IgG noma kwe-IgM.

Ukutholwa

I-COVID-19 IgG/IgM Rapid Test Device (Igazi Eliphelele/iSerum/Plasma) iwukuhlolwa kwe-lateral flow immunechromatographic ukuze kutholwe amasosha omzimba e-IgG kanye ne-IgM ku-2019-nCoV egazini lonke, i-serum noma isampula se-plasma.

Isifanekiso

Igazi eliphelele, i-Serum noma i-Plasma specimen.

Ukunemba

Umphumela we-IgG:

Ukuzwela Okuhlobene: 98.28%

Ukucaciswa okuhlobene: 97.01%

Ukunemba:97.40%

Umphumela we-IgM:

Ukuzwela Okuhlobene: 82.76%

Ukucaciswa okuhlobene: 98.51%

Ukunemba: 93.75%

Isikhathi Semiphumela

Funda imiphumela ngemizuzu eyi-15 futhi ungabi ngaphezu kwemizuzu engama-30.

Izimo zokugcina ikhithi

2~30°C.

Okuqukethwe

  P231133 P231134 P231135
Idivayisi yokuhlola i-COVID-19 IgG/IgM ama-pcs angu-40 30 ama-pcs 1 ngakunye
Isampula sebhafa 5mL/Bot.1Bot 80μl/ibhodlela30 ibhodlela  80μl/ibhodlela1 isitsha
I-Capillary dropper* ama-pcs angu-40 30 ama-pcs 1 ngakunye
Faka iphakheji 1 ngakunye 1 ngakunye 1 ngakunye

*I-Capillary dropper: Ngegazi lonke.

Uku-oda Ulwazi

Umkhiqizo

Ikati.No.

Okuqukethwe
KaiBiLiTMI-COVID-19 IgG/IgM P231133 Izivivinyo ezingama-40
KaiBiLiTMI-COVID-19 IgG/IgM P231134 Izivivinyo ezingama-30
KaiBiLiTMI-COVID-19 IgG/IgM P231135 1 Izivivinyo
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