HWTS-RT065A/B/C/D-COVID-19 /Flu A &B/ RSV/ADV Ag Combo Rapid Test

Inkcazo emfutshane:

Le khithi yenzelwe ukubhaqa ii-antigens ze-SARS-CoV-2, i-Influenza virus A kunye ne-B, i-Respiratory Syncytial Virus, kunye ne-Adenovirus kwisampuli ze-nasal swabs ezivela kubarhanelwa ukuba banentsholongwane zingadlulanga iintsuku ezi-7 emva kokuqala kweempawu kunye nokudibana okusondeleyo ekuxilongweni okwahlukileyo kwentsholongwane yendlela yokuphefumla yi-SARS-CoV-2, i-Influenza Virus A kunye ne-B, i-Respiratory Syncytial Virus, kunye ne-Adenovirus. Iziphumo zovavanyo akufuneki zisetyenziswe njengesiseko sodwa sesigqibo seklinikhi sokuxilonga kunye nonyango. Ukuxilongwa okungakumbi kweklinikhi kufuneka kuqinisekiswe ngeendlela ezahlukeneyo zovavanyo kunye nezinye iziphumo zeklinikhi. Le khithi yenzelwe ukusetyenziswa kwe-in vitro kuphela kwaye ayizenzekeli.


Iinkcukacha zeMveliso

Iithegi zeMveliso

Igama lemveliso

HWTS-RT065A/B/C/D-COVID-19 /Flu A &B/ RSV/ADV Ag Combo Rapid Test

Ukuvunywa kweMveliso

CE3018 (IVDR)

Imigaqo yovavanyo

Le khithi isebenzisa iteknoloji ye-immunochromatography kwindlela yesandwich ye-double-antibodyukufumanisa ii-antigens ze-SARS-CoV-2, i-Influenza virus A kunye ne-B, i-Respiratory SyncytialIintsholongwane, kunye ne-Adenovirus. Umcu wovavanyo wawugqunywe ngee-antibodies ezithile ukwenza uvavanyoimigca ye-pathogen ekujoliswe kuyo. Ngexesha lovavanyo, isampuli elungisiweyo eza kuvavanywayongezwe kwiqula lesampulu yeekhasethi zoVavanyo. Xa isampulu eza kuvavanywa iqulethei-pathogen ekujoliswe kuyo xa iphezulu kune-LoD, i-antigen ekujoliswe kuyo kunye ne-I-antibody ehambelanayo ebhalwe ilebhile iya kwenza i-reaction compound. Phantsi kwesenzoye-chromatography, i-reaction compound iya phambili nge-nitrocellulosei-membrane, ihlangana kumgca wovavanyo kwaye ekugqibeleni yenza ibhendi ebomvu, ebonisa ukuba ilungileyentsholongwane yovavanyo ehambelanayo. Ngokwahlukileyo koko, ukuba isampuli ayinayo injongoi-pathogen okanye uxinaniso lwe-antigen luphantsi kune-LoD, akukho band ebomvu iya kuvela kwiumgca wovavanyo, obonisa ukuba akukho ntsholongwane ifanelekileyo yovavanyo. Nokubakukho intsholongwane ekujoliswe kuyo kwisampulu, kufuneka kubekho ibhendi ebomvu xa kulawulwa umgangatho.umgca (C), osebenza njengolawulo lwangaphakathi lokujonga inkqubo ye-chromatography kunyeikhithi yovavanyo iyasebenza.

Iiparameters zobugcisa

Indawo yokugcina izinto 4-30°C
Beka ubomi kwishelufa Iinyanga ezingama-24
Uhlobo lweSibonelelo I-swab yempumlo
Ixesha lokufunyaniswa Imizuzu eli-15-20

Iimpawu zokusebenza

2

Ukuhamba komsebenzi

3
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