Inyathelo elinye Ukuchaneka okuphezulu kweCE evunyiweyo kwekhithi yoVavanyo lweMalaria Pf/Pan

Uvakalelo

I-Malaria Pf/Pan Rapid Test Device (Igazi Elipheleleyo) ivavanyiwe ngemakroskopu ebhityileyo okanye engqindilili kwiisampulu zeklinikhi.Iziphumo zibonisa ukuba ubuntununtunu beMalaria Pf/Pan Rapid Test Device (Igazi Elipheleleyo) yi>99.9% xa kuthelekiswa nemicroscope.
YePani:
Uvakalelo olunxulumeneyo: >99.9% (103/103) (96.5%～100.0%)*
YePf:
Uvakalelo olunxulumeneyo: >99.9% (53/53) (93.3%～100.0%)*

Ukuchaza ngokuthe ngqo

I-Malaria Pf/I-Pan Rapid Test Device (iGazi Elipheleleyo) isebenzisa izilwa-buhlungu ezikhethekileyo zeMalaria Pf/Pan antigens egazini lilonke.Iziphumo zibonisa ukuba ubume beMalaria Pf/Pan Rapid Test Device (Igazi Elipheleleyo) ingaphezulu kwama-99.0% xa kuthelekiswa nemicroscope.
Iinkcukacha Ngokuhambelanayo: 99.1% (213/215)(96.7%～99.9%)*
Ukuchaneka: 99.4% (359/361)(98.0%～99.9%)*
* 95% iThutyana lokuzithemba

Phawula:Uthelekiso lwePan line lwenziwe kuphela ngeesampulu zegazi ezine-Plasmodium vivax specimen.Amabango ePan lines asekelwe kwiziphumo zenzululwazi zokuba iPan-malarial Lactate Dehydrogenase ifumaneka kwezinye iiparasite zemalariya eziquka iPlasmodium ovale kunye nePlasmodium malariae.

UKUSETYENZISWA OKUHLOSIWEYO

I-Malaria Pf/Pan Rapid Test Device (Igazi Elipheleleyo) luvavanyo lwe-chromatographic olukhawulezayo lokukhangela umgangatho we-antigens ejikelezayo ye-Plasmodium falciparum, i-Plasmodium vivax, i-Plasmodium ovale, i-Plasmodium malariae egazini lonke.

Inzuzo yeNkampani

1.Umvelisi oyiNgcali, ishishini “eliphambili” elikwinqanaba lesizwe.
2.Hambisa iimpahla njengesicelo somyalelo
3.ISO13485, CE, Lungisa amaxwebhu ahlukeneyo okuthumela
4.Phendula imibuzo yabathengi kwiiyure ezingama-24