Test Diagnostic Medical Device CE yakanyorwa Syphilis Test kit

ZVAKANAKA:* Mitsetse miviri inooneka.Mutsetse mumwe weruvara unofanirwa kunge uri munharaunda yekudzora mutsara (C) uye imwe mutsara unoonekera weruvara unofanirwa kunge uri munharaunda yebvunzo (T).
*Cherechedza: Kusimba kweruvara munharaunda yebvunzo (T) kuchasiyana zvichienderana nekuwanda kwemasoja ekudzivirira eTP aripo mumuenzaniso.Naizvozvo, chero mumvuri weruvara munharaunda yebvunzo (T) inofanirwa kutorwa seyakanaka.

NEGATIVE: Mutsara mumwe wemavara unoonekwa munharaunda yekutonga (C).Hapana mutsara unowanikwa munharaunda yebvunzo (T).

INVALID: Mutsetse wekudzora watadza kuoneka.Kusakwana specimen vhoriyamu kana zvisirizvo maitiro emaitiro ndizvo zvinonyanya zvikonzero zvekutadza kwekudzora mutsara.Ongorora maitiro uye dzokorora bvunzo nebvunzo nyowani.Kana dambudziko rikaramba riripo, regedza kushandisa test kit nekukasira uye ubate mushambadzi wenzvimbo yako.

Clinical Sensitivity, Kunyatsojeka uye Kururama
Ongororo yeSyphilis Rapid Test (Ropa Rakazara/Serum/Plasma) yakaratidza nenzira kwayo zvienzaniso zveseroconversion panel uye yakafananidzwa neinotungamira kutengeserana TPHA Syphilis bvunzo uchishandisa sampuli dzekiriniki.Zvabuda zvinoratidza kuti kunzwisiswa kweiyo The Syphilis Rapid Test Device (Whole Ropa/Serum/Plasma) i99.5% uye hukama hwacho i99.3%.

Syphilis Rapid Test vs. TPHA

Kunzwira tsitsi: 99.5% (98.2% -99.9%)*
Hukama chaihwo: 99.3% (98.1% -99.8%)*
Kururama: 99.4% (98.6% -99.8%)*
* 95% Kuvimba Nenguva

ZVIRI KUSHANDISA

Iyo Syphilis Rapid Test (Ropa Rakazara/Serum/Plasma) inokurumidza chromatographic immunoassay yemhando yekuona masoja ekudzivirira chirwere (IgG neIgM) kusvika kuTreponema Pallidum (TP) muropa rose, serum kana plasma kubatsira mukuongororwa kweSyphilis.

Kubatsira kwedu

1.Professional Manufacturer, nyika-yepamusoro-soro tekinoroji "giant" bhizinesi.
2.Deliver zvinhu sechikumbiro chekuraira
3.ISO13485, CE, Gadzirira zvinyorwa zvakasiyana-siyana zvekutumira
4.Reply vatengi mibvunzo mukati maawa 24