High accuracy Infectious Disease Typhoid Test kit

Clinical Performance YeIgM Muedzo
Huwandu hwemasamples 334 kubva kune vanobatwa nenjodzi akaongororwa neTyphoid Antibody Rapid Test uye neyekutengesa S. typhi IgM EIA.Kuenzanisa kwezvidzidzo zvese kunoratidzwa mutafura inotevera.

Relative Sensitivity: 91.2% (76.3% - 98.1%)*
Kunyanya Kukosha: 99.3% (97.6% - 99.9%) *
Hukama Hwakarurama: 98.5% (96.5% - 99.5%)*
* 95% Kuvimba Nenguva

Clinical Performance YeIgG Muedzo
Huwandu hwemasamples 314 kubva kune vanobatwa nenjodzi akaongororwa neTyphoid Antibody Rapid Test uye neyekutengesa S. typhi IgG EIA kit.Kuenzanisa kwezvidzidzo zvese kunoratidzwa mutafura inotevera.

Relative Sensitivity: 92.9% (66.1% - 99.8%)*
Kunyanya Kukosha: 99.3% (97.6% - 99.9%) *
Hukama Hwakarurama: 99.0% (97.2% - 99.8%)*
* 95% Kuvimba Nenguva

ZVIRI KUSHANDISA

Iyo Typhoid Antibody Rapid Test Device ndeye lateral kuyerera immunoassay yekuona panguva imwe chete uye kusiyanisa anti-Salmonella typhi (S. typhi) IgG uye IgM muropa revanhu rose, serum kana plasma.Inotarisirwa kushandiswa semuongorori wekuongorora uye seyamuro mukuongororwa kwechirwere cheS typhi.Chero reactive sampuli ine Typhoid Antibody Rapid Test inofanirwa kusimbiswa neimwe nzira yekuyedza (s).

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