Ukuchaneka okuphezulu Ikiti yoVavanyo lweSifo esosulelayo seTyphoid

Ukusebenza kweKlinikhi kuVavanyo lwe-IgM
Zizonke iisampulu ezingama-334 ezisuka kwizifundo ezisesichengeni ziye zavavanywa yiTyphoid Antibody Rapid Test kunye neS. typhi IgM EIA yorhwebo.Ukuthelekisa zonke izifundo kuboniswe kolu luhlu lulandelayo.

I-Relative Sensitivity: 91.2% (76.3% - 98.1%)*
Inkcazo ngokunxulumene: 99.3% (97.6% - 99.9%) *
Ukuchaneka okuNxulumeneyo: 98.5% (96.5% - 99.5%)*
* I-95% yamaxesha okuzithemba

Ukusebenza kweKlinikhi kuVavanyo lwe-IgG
Zizonke iisampulu ezingama-314 ezivela kwizifundo ezichaphazelekileyo ziye zavavanywa yiTyphoid Antibody Rapid Test kunye nekhithi yorhwebo ye-S. typhi IgG EIA.Ukuthelekisa zonke izifundo kuboniswe kolu luhlu lulandelayo.

I-Relative Sensitivity: 92.9% (66.1% - 99.8%)*
Inkcazo ngokunxulumene: 99.3% (97.6% - 99.9%) *
Ukuchaneka okuNxulumeneyo: 99.0% (97.2% - 99.8%)*
* I-95% yamaxesha okuzithemba

UKUSETYENZISWA OKUHLOSIWEYO

I-Typhoid Antibody Rapid Test Device yi-lateral flow immunoassay yokufumanisa ngaxeshanye kunye nokwahlukana kwe-anti-Salmonella typhi (S. typhi) IgG kunye ne-IgM kwigazi elipheleleyo lomntu, i-serum okanye i-plasma.Yenzelwe ukuba isetyenziswe njengovavanyo lokuhlola kwaye njengoncedo ekuxilongeni usulelo nge-S. typhi.Nawuphi na umzekelo osebenzayo kunye noVavanyo oluKhawulezayo lweTyphoid Antibody kufuneka luqinisekiswe ngenye indlela yovavanyo.

Inzuzo Yethu

1.Eyaziwa njengeshishini lobuchwepheshe obuphezulu eTshayina, inani lezicelo zamalungelo awodwa abenzi kunye namalungelo okushicilela esoftware yamkelwe.
2.Hambisa iimpahla njengesicelo somyalelo
3.ISO13485, CE, Lungisa amaxwebhu ahlukeneyo okuthumela
4.Phendula imibuzo yabathengi kwiiyure ezingama-24