Ukusetyenziswa kwezonyango ikiti yoVavanyo lweTyphoid yobuchwephesha, inyathelo elinye lovavanyo olukhawulezayo ikhasethi eFakelweyo Umfanekiso

Ukusetyenziswa kwezonyango kwikiti yoVavanyo lweTyphoid, inyathelo elinye lovavanyo olukhawulezayo lwekhasethi

Inkcazelo emfutshane:

Iinkcukacha zeMveliso

Iithegi zeMveliso

Uvakalelo lweKlinikhi, Ukuchaneka nokuchaneka

Uvavanyo lwe-Influenza A+B Antigen Rapid Test luvavanyiwe xa luthelekiswa ne-RT-PCR.I-539 ye-nasopharyngeal swabs kunye ne-oropharyngeal swabs zavandlakanywa kunye novavanyo olukhawulezayo lwe-Influenza A + B.

Izinto	Ukugxila	Izinto	Ukugxila
Ukutshiza ngeempumlo	15% v/v	IHemoglobin	10% v/v
Mucin	0.5 % w/v	Mupirocin	10 mg/mL
Amathontsi ngeempumlo	15% v/v	Ukuhlamba imilomo	/
I-Chloraseptic	1.5 mg/mL	Levofloxacin	40 ug/mL
I-Oseltamivir	2ug/mL	I-Ribavirin	0.2ug/mL
I-Fluticasone propionate	5% v/v	Ceftriaxone	800 ug/mL
Tobramycin	4ug/mL	I-Saline yeeNcinci zokutshiza	10% v/v

NgoMkhuhlane A

Indlela		I-RT-PCR		Zizonke iziphumo
Uvavanyo loMkhuhlane A+B oluKhawulezayo	Iziphumo	Okuhle	Ibi	Zizonke iziphumo
	Okuhle	116	1	117
	Ibi	5	417	422
Zizonke iziphumo		121	418	539

Uvakalelo lweklinikhi: 95.87% (95% CI: 90.69% ~ 98.22%)
Ubungcali beklinikhi: 99.76% (95% CI: 98.66% ~ 99.96%)
Ireyithi yeNxulumano iyonke: 98.89% (95% CI: 97.59% ~ 99.49%).

NgoMkhuhlane B:

Indlela		I-RT-PCR		Zizonke iziphumo
Uvavanyo loMkhuhlane A+B oluKhawulezayo	Iziphumo	Okuhle	Ibi	Zizonke iziphumo
	Okuhle	97	1	98
	Ibi	6	435	441
Zizonke iziphumo		103	436	539

Uvakalelo lweklinikhi: 94.17% (95% CI: 87.87% ~ 97.30%)
Ubungcali beklinikhi: 99.77% (95% CI: 98.71% ~ 99.96%)
Ireyithi yeNxulumaniso iyonke: 98.70% (95% CI: 97.34% ~ 99.37%).

Uvakalelo lokuHlalutya/LOD

Hangzhou Aichek Medical Technology CO., Ltd.

Jinxing Cun, Yuhang Community, Yuhang

ISithili (IsiXeko seSayensi seNzululwazi yekamva), iHangzhou,

Zhejiang, PR China

SUNGO Europe BV

I-Olympisch Stadion 24, 1076DE Amsterdam, Netherlands

Umda wokubhaqwa (LOD) ichongiwe ngokuvavanywa koxinzelelo olwahlukileyo lwentsholongwane yomkhuhlane A kunye nentsholongwane yomkhuhlane B kuMkhuhlane A+B we-Antigen Rapid Test.Ugxininiso oluchongwe njengamanqanaba eLOD avavanyiweyo zidweliswe ngezantsi.
Umkhuhlane A (H3N2): 5×103 TCID50/mL
Umkhuhlane A (H1N1): 2.5×103 TCID50/mL
Umkhuhlane A (H1N1 pdm09): 2.5×103 TCID50/mL
Umkhuhlane B (Yamagata): 3.5×103 TCID50/mL
I-Influenza B (i-Victoria): 1.0 × 103 TCID50 / mL

Ukuchaneka koHlahlo (Ukuphinda kusebenze kwakhona ngokunqamlezayo)

Ukumisela uhlalutyo oluthile lwe-Influenza A + B ye-Antigen Rapid Test, ii-microorganisms ezininzi ze-commensal okanye ze-pathogenic ezinokubakho kwindlela yokuphefumula ephezulu zavavanywa.
Iisampulu ezintle nezimbi zaye zajongwa ngezi ntsholongwane zavavanywa kuxinaniso lwe-106 TCID50/mL, kubandakanywa i-SARS-CoV-2, i-Human coronavirus HKU1, OC43, NL63, 229E, MERS, Rhinovirus, Adenovirus, Enterovirus, Metapneumotoryeumovirus, iParainflunza, iParainflunza syncytial virus, Mycoplasma pneumonia, Chlamydia pneumonia, Streptococcus pneumonia, Staphylococcus aureus, Mycobacterium tuberculosis, Haemophilus influenzae, Streptococcus pyogenes.Akukho kuphinda kusebenze kwakhona kubonwe ngoMkhuhlane A+B Antigen Rapid Test.

UKUSETYENZISWA OKUHLOSIWEYO

Umkhuhlane A+B Antigen Rapid Test is a lateral flow immunoassay eyenzelwe ukufunyaniswa komgangatho womkhuhlane A kunye neantigens zomkhuhlane B kwiswab ye-nasopharyngeal kunye ne-oropharyngeal swab.

Inzuzo yeNkampani

1. UMvelisi oyiNgcali, ishishini “eliphambili” elikwinqanaba lesizwe
2.Hambisa iimpahla njengesicelo somyalelo
3.ISO13485, CE, Lungisa amaxwebhu ahlukeneyo okuthumela
4.Phendula imibuzo yabathengi kwiiyure ezingama-24

Ngaphambili: CE ivunyiwe H. Pylori Ag Rapid Test kit, uvavanyo Cassette

Okulandelayo: Inyathelo elinye eliphezulu lokuchaneka kweMalaria Pf/Pv Test kit

Bhala umyalezo wakho apha kwaye uwuthumele kuthi