UVavanyo oluKhawulezayo lwe-SARS-CoV-2 ye-Antigen (i-Colloidal Gold) yokuzivavanya

I-SARS-CoV-2 Antigen Rapid Test (i-Colloidal Gold) yokuzivavanya yenzelwe ukufunyaniswa okusemgangathweni kwe-SARS-CoV-2 Antigen (iprotein ye-Nucleocapsid) kwiisampulu zamathe omntu kwi-vitro.

Ezi zisetyenziswa kwezi meko zilandelayo:

1. Ukuhlolwa kobuninzi babantu, njengesibhedlele, isikhululo seenqwelomoya, isikhululo, uluntu, njl.

2. ucupho oluqhubekayo lwexesha elifutshane.

• Isampulu yempumlo yangaphambili, ayivaleli

* Kulula kakhulu ukuyisebenzisa

* Kulula, akukho sixhobo sifunekayo

* Ngokukhawuleza, iziphumo ngaphakathi kwe-15 ~ 20 imizuzu

* Ukonga iindleko

Intsholongwane ye-SARS-CoV-2 yenziwe ngamacandelo amahlanu: ikhonkco lemfuza ye-RNA kunye neeproteni ezine. Umgangatho ongaphandle we-particle yi-Spike Protein (S), kunye ne-Envelope yentsholongwane engaphantsi kwe-Spike yenziwe nge-Envelope Protein (E) kunye ne-Membrane Protein (M). Undoqo oqulethwe ngaphakathi kwemvulophu sisakhiwo esigoqiweyo se-helical esakhiwe ngamaketanga emfuza e-RNA kunye neeprotheni ze-Nucleocapsid (N). Usebenzisa umgaqo wokubophelela okukhethekileyo kwe-antigen kunye ne-antibody, ubukho be-antigen ye-SARS-CoV-2 (iprotein ye-Nucleocapsid) inokubonwa li-antibody.

Izinto eziluncedo phezu Elisa kunye PCR

Ukusebenza kwe-SARS-CoV-2 Antigen Rapid Test (Colloidal Gold) yasekwa kunye nemizekelo engama-859 eqokelelwe kwizigulane ezineempawu ezirhanelwa ukuba zine-COVID-19. Iisampulu zangaphambili zeempumlo ze-swab zaqokelelwa kwaye zavavanywa ngokweemfuno zeMiyalelo yokuSetyenziswa. Ukugcinwa, ukuthuthwa kunye nokufunyanwa kweesampuli emva kokuqokelela kudibene neemfuno ezifanelekileyo zeMiyalelo yokusetyenziswa. Kwangelo xesha, i-SARS-CoV-2 yabhaqwa yimeko yongxamiseko yokufumanisa i-nucleic acid.

Isishwankathelo sokusebenza konyango lwe-WIZ'S SARS-CoV-2 Antigen Rapid Test (Colloidal Gold)

I-PPA: 95.91% (C.I. 93.25% ~ 97.55%)

I-NPA: 100.00% (C.I. 99.26% ~ 100.00%)

OPA: 98.37% (C.I. 97.28% ~ 99.03%)

Thina, umenzi, ngoku, sibhengeza ukuba i(i)mveliso njengoko ichaziwe ngasentla iyahlangabezana nemimiselo esebenzayo yoMyalelo waseYurophu 98/79/EC kwi-in vitro Diagnostic Medical Devices. Onke amaxwebhu obugcisa axhasayo abonisa ukuthotyelwa agcinwa ngumenzi kwaye angenziwa afumaneke nguMmeli oGunyaziweyo eYurophu.

Isiqinisekiso seNkampani

Iprofayile yekhampani

Umboniso weNkampani

A:Zombini.Siye kule ntsimi ngaphezulu kwe-7years.Ngeemveliso ezikumgangatho ophezulu kunye nexabiso elikhuphisanayo, sinethemba elinyanisekileyo lokuphuhlisa ishishini elixhamlayo kunye nabathengi bethu kwihlabathi liphela.

A: T/T,L/C,D/A,D/P njalo njalo.

A: EXW, FOB, CFR, CIF, DDU njalo njalo.

A: Ngokuqhelekileyo, kuya kuthatha i-15 kwiintsuku ze-30 emva kokufumana idiphozithi Ixesha elithile lokuhambisa lixhomekeke kwizinto kunye nobuninzi bomyalelo wakho.

A: Ewe, sinokuvelisa ngeesampuli zakho okanye imizobo yobugcisa.

A: Ukuba ubungakanani buncinci, iisampuli ziya kukhululeka, kodwa abathengi kufuneka bahlawule iindleko ze-courier.

A: Ewe, sinovavanyo lwe-100% ngaphambi kokunikezelwa.

A: Sigcina umgangatho olungileyo kunye nexabiso elikhuphisanayo ukuqinisekisa ukuba abathengi bethu bayazuza; kwaye sihlonipha wonke umthengi njengomhlobo wethu kwaye siqhuba ishishini ngokunyanisekileyo kwaye senze ubuhlobo nabo.