Karete ea Teko e Potlako ea COVID-19 Antigen (Colloidal Gold)

COVID-19 Antigen Rapid Test Card (Colloidal Gold) e reretsoe ho lemoha boleng ba SARS-CoV-2 Antigen (Nucleocapsid protein) lisampoleng tsa mathe a motho in vitro.

E sebelisoa maemong a latelang:

1. tlhahlobo ea bongata ba batho, joalo ka sepetlele, boema-fofane, seteishene, sechaba, joalo-joalo.

2. boalosi bo sa khaotseng ba nakoana.

* Mohlala o ka pele oa nasal swab, ha o hlaselehe

* Ho bonolo haholo ho e sebelisa

* E bonolo, ha ho sesebelisoa se hlokahalang

* E potlakile, e fella ka metsotso e 15-20

* E boloka litšenyehelo

Karolo ea vaerase ea SARS-CoV-2 e entsoe ka likarolo tse hlano: ketane ea lefutso ea RNA le liprotheine tse 'ne. Karolo e ka ntle ea karoloana ke Spike Protein (S), 'me Enfelopo ea kokoana-hloko e ka tlaase ho Spike e entsoe ka Envelope Protein (E) le Membrane Protein (M). Moko-taba o ka har'a enfelopo ke sebopeho se phuthetsoeng sa helical se entsoeng ka liketane tsa liphatsa tsa lefutso tsa RNA le liprotheine tsa Nucleocapsid (N). U sebelisa molao-motheo oa ho tlama ha antigen le antibody, boteng ba SARS-CoV-2 antigen (Nucleocapsid protein) bo ka bonoa ke antibody.

Melemo ho feta Elisa le PCR

Ts'ebetso ea SARS-CoV-2 Antigen Rapid Test (Colloidal Gold) e thehiloe ka mehlala e 859 e neng e tla bokelloa ho tsoa ho bakuli ba nang le matšoao ba neng ba belaelloa ka COVID-19. Mehlala e ka pele ea nasal swab e ile ea bokelloa le ho lekoa ho latela litlhoko tsa Litaelo tsa Tšebeliso. Ho boloka, ho tsamaisa le ho lemoha lisampole ka mor'a ho bokelloa li ile tsa kopana le litlhoko tse nepahetseng tsa Litaelo tsa Tšebeliso. Ka nako e ts'oanang, SARS-CoV-2 e ile ea bonoa ke ts'ebetso ea tšohanyetso ea nucleic acid.

Kakaretso ea ts'ebetso ea tleliniki ea WIZ'S SARS-CoV-2 Antigen Rapid Test (Colloidal Gold)

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

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

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

Rōna, moetsi, mona, re phatlalatsa hore sehlahisoa(li)hlahisoa joalo ka ha se boletsoe ka holimo se kopana le(li) lipehelo tse sebetsang tsa European Directive 98/79/EC on in vitro Diagnostic Medical Devices. Litokomane tsohle tse tšehetsang tsa tekheniki tse bonts'ang ho latela melao li bolokoa ke moetsi 'me li ka fumaneha ke Moemeli ea Fetohetseng Europe.

Setifikeiti sa Khampani

Boemo ba Khoebo

Pontšo ea Khampani

A: Both.Re bile tšimong ena ka nako e fetang 7years. Ka lihlahisoa tsa boleng bo phahameng le theko ea tlhōlisano, re na le tšepo e tiileng ea ho ntshetsa pele khoebo e nang le melemo le bareki ba rona lefatšeng ka bophara.

A: T/T,L/C,D/A,D/P joalo-joalo.

A: EXW, FOB, CFR, CIF, DDU joalo-joalo.

A: Ka tloaelo, ho tla nka matsatsi a 15 ho isa ho a 30 ka mor'a ho amohela depositi Nako e khethehileng ea ho fana ka thepa e itšetlehile ka lintho le bongata ba taelo ea hau.

A: E, re ka hlahisa ka mehlala ea hau kapa litšoantšo tsa theknoloji.

K: Haeba palo e le nyane, lisampole li tla ba mahala, empa bareki ba tlameha ho lefa litšenyehelo tsa ho tsamaisa thepa.

A: E, re na le teko ea 100% pele re pepa.

A: Re boloka boleng bo botle le theko ea tlholisano ho netefatsa hore bareki ba rona ba rua molemo; hape re hlompha moreki e mong le e mong joalo ka motsoalle oa rona mme re etsa khoebo ka tieo le ho etsa setsoalle le bona.