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Idivayisi yokuhlola esheshayo ye-COVID-19 Ag

Idivayisi yokuhlola esheshayo ye-COVID-19 Ag

I-SARS-COV-2 Antigen Rapid Test Device iyisivivinyo esisheshayo esibonakalayo sokutholwa kwekhwalithi, okucatshangelwayo kwama-antigen e-COVID-19 enza ama-swabs omphimbo kanye nama-nasopharyngeal swab specimens.

Kuhloswe ukuthi kusetshenziswe ochwepheshe njengokuhlola futhi inikeza umphumela wokuhlola wokuqala ukusiza ekuxilongeni ukutheleleka nge-coronavirus yenoveli.

Noma yikuphi ukuhunyushwa noma ukusetshenziswa kwalo mphumela wokuhlolwa kokuqala kufanele futhi kuncike kokunye okutholwe emitholampilo kanye nokwahlulela kochwepheshe kwabahlinzeki bezempilo.Enye indlela(izindlela) zokuhlola kufanele icatshangelwe ukuze kuqinisekiswe umphumela wokuhlolwa otholwe yilolu hlolo.


Imininingwane Yomkhiqizo

Omaka bomkhiqizo

IZINTO ZEKHITHI

20 test cassette
20 ama-swabs oyinyumba
20 isilondolozi sokukhipha okukodwa
1 iphakheji efakiwe
1 inkomba esheshayo

INGCACISO YOMKHIQIZO

Ibhrendi Funworld Isitifiketi CE, ISO13485
Isifanekiso I-Nasopharyngeal swabs/ I-swab yamakhala Okuqukethwe Ikhasethi , Buffer , ama-swabs oyinyumba Faka iphakheji
Isikhathi sokufunda Imizuzu eyi-10 Pakisha 20 T
Isitoreji 2-30 ℃ Impilo yeshelufu iminyaka engu-2

UKU-ODA ULWAZI

Incazelo yomkhiqizo Isifanekiso Ifomethi Pakisha Isitifiketi
Ukuhlolwa Okusheshayo kwe-SARS-COV-2 Antigen I-Nasopharyngeal swabs/ I-swab yamakhala Ikhasethi 20 T CE, ISO13485
I-COVID-19 Antigen Rapid Test I-Nasopharyngeal swabs/ I-swab yamakhala Ikhasethi 20 T CE, ISO13485
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UKUGCINWA NOKUZInza

Ikhithi kufanele igcinwe ku-2-30 ° C kuze kube usuku lokuphelelwa yisikhathi luphrintiwe esikhwameni esivaliwe.

Ukuhlolwa kufanele kuhlale esikhwameni esivaliwe kuze kusetshenziswe.

Ungaqandi.

Kufanele kuqashelwe ukuvikela izingxenye zekhithi ekungcoleni.Ungasebenzisi uma kunobufakazi bokungcoliswa kwamagciwane noma imvula.Ukungcoliswa kwebhayoloji kwezinto ezisetshenziswayo zokusaphaza, iziqukathi noma ama-reagents kungaholela emiphumeleni engamanga.


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