SARS-CoV-2 Antigen Rapid Test (Colloidal Gold)

SARS-CoV-2 Antigen Rapid Test (Colloidal Goridhe) yakagadzirirwa kuongororwa kwemhando yeSARS-CoV-2 Antigen (Nucleocapsid protein) mumasampuli emate emunhu mu vitro.

Izvo zvinoshandiswa kune zvinotevera zviitiko:

1. kuongororwa kwehuwandu hwevanhu, sechipatara, airport, chiteshi, nharaunda, nezvimwe.

2. kutariswa kwenguva pfupi kunoramba kuripo.

* Anterior nasal swab specimen, isingasviki

* Yakanyanya nyore kushandisa

* Yakanaka, hapana chiridzwa chinodiwa

* Nekukurumidza, mhedzisiro mukati me15 ~ 20 maminetsi

* Mari-inoshanda

SARS-CoV-2 Antigen Rapid Test (Colloidal Gold)

Iyo SARS-CoV-2 hutachiona chidimbu inoumbwa nezvikamu zvishanu: RNA gene cheni uye mana mapuroteni. Iro rekunze rechikamu iSpike Protein (S), uye Viral Envelope iri pazasi peSpike inoumbwa neEmvuropu Protein (E) uye Membrane Protein (M). Iyo yakakosha iri mukati mehamvuropu ndeye helical yakapetwa chimiro chinoumbwa neRNA gene cheni uye Nucleocapsid mapuroteni (N). Uchishandisa musimboti wekusunga chaiko kweantigen uye antibody, kuvapo kweSARS-CoV-2 antigen (Nucleocapsid protein) inogona kuwonekwa neanorwisa matutu.

Zvakanakira pamusoro paElisa uye PCR

Kuita kweSARS-CoV-2 Antigen Rapid Test (Colloidal Goridhe) yakavambwa iine mazana masere nemakumi mashanu nematatu emhando dzakaunganidzwa kubva kuvarwere vane zviratidzo vaifungidzirwa kuti vane COVID-19. Anterior nasal swab specimens akaunganidzwa uye akaedzwa maererano nezvinodiwa zveMirairo Yekushandisa. Kuchengetwa, kutakurwa uye kucherechedzwa kwemasampuli mushure mekuunganidzwa kwakasangana nezvinodiwa zveMirairo Yekushandisa. Panguva imwecheteyo, SARS-CoV-2 yakaonekwa ne emergency nucleic acid yekuona reagent.

Clinical performance pfupiso yeSARS-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%)

Isu, mugadziri, pano, tinozivisa kuti chigadzirwa (s) sezvakatsanangurwa pamusoro zvinosangana nezvinodiwa zveEuropean Directive 98/79/EC pa in vitro Diagnostic Medical Devices. Ese anotsigira magwaro ehunyanzvi anoratidza kutevedzera anochengetwa nemugadziri uye anogona kuitwa kuti awanikwe neMumiriri Akabvumidzwa muEurope.

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Q1. Iwe uri fekitori kana kambani yekutengesa?

A: Both.Tanga tiri mundima iyi kweanopfuura 7years.Nezvigadzirwa zvepamusoro zvemhando yepamusoro uye mutengo wemakwikwi, tinotarisira nomwoyo wose kukudziridza bhizinesi rinobatsirana nevatengi vedu pasi rose.

Q2. Ndeipi mitemo yako yekubhadhara?

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

Q3. Ndeipi mitemo yako yekutumira?

A: EXW, FOB, CFR, CIF, DDU uye zvichingodaro.

Q4. Zvakadini nenguva yekuendesa yeSARS-CoV-2 Antigen Rapid Test (Colloidal Gold)?

A: Kazhinji, zvinotora 15 kusvika 30 mazuva mushure mekugamuchira dhipoziti Nguva chaiyo yekuendesa inobva pane zvinhu uye uwandu hwekuraira kwako.

Q5. Unogona kuronga kugadzirwa zvinoenderana nemasampuli?

A: Hongu, tinogona kugadzira nemasampuli ako kana hunyanzvi kudhirowa.

Q6. Ndeupi mutemo wako wemuenzaniso?

A: Kana huwandu hwacho huri hudiki, masampula anove emahara, asi vatengi vanofanirwa kubhadhara mutengo wekutumira.

Q7. Unoyedza zvinhu zvako zvese usati wazvitakura here?

A: Hongu, tine 100% bvunzo tisati tasvika.

Q8. Iwe unoita sei bhizinesi redu kwenguva refu uye hukama hwakanaka?

A: Isu tinochengeta kunaka kwakanaka uye mutengo wemakwikwi kuti tive nechokwadi chekuti vatengi vedu vanobatsirwa; uye tinoremekedza mutengi wese seshamwari yedu uye tinoita bhizinesi nemoyo wese uye kuita hushamwari navo.