Testsea Disease Test H.pylori Ab Rapid Test Kit

Inkcazelo emfutshane:

I-Helicobacter pylori (H. pylori) luhlobo lweebhaktheriya ezichaphazela umgca wesisu, ngokuqhelekileyo zihambelana neemeko zesisu ezifana nezilonda ze-peptic, i-gastritis engapheliyo, kwaye kwezinye iimeko, kwandisa umngcipheko womhlaza wesisu. I-H. pylori ilungelelaniswe kakhulu ukuze iphile kwindawo ene-asidi yesisu, apho inokubangela ukuvuvukala kunye nomonakalo kwisisu sesisu.

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Iinkcukacha zeMveliso

Iithegi zeMveliso

Iinkcukacha eziKhawulezayo

Igama lebrand:	Testsea	Igama lemveliso:	Uvavanyo lwe-H.Pylori Ab
Indawo yemvelaphi:	Zhejiang, China	Uhlobo:	Izixhobo zokuHlalutya kwePathological
Isatifikethi:	CE/ISO9001/ISO13485	Ukuhlelwa kwesixhobo	Udidi III
Ukuchaneka:	99.6%	Umzekelo:	Igazi Elipheleleyo/iSerum/Plasma
Ubume:	Ikhasethi	Inkcazo:	3.00mm/4.00mm
MOQ:	1000 iiPC	Beka ubomi kwishelufa:	iminyaka eyi-2
OEM & ODM	inkxaso	Inkcazo:	40pcs / ibhokisi

Supply Ability:

5000000 Iqhekeza/Amaqhekeza ngenyanga

Ukupakishwa kunye nokuhanjiswa:

Iinkcukacha zokuPakisha

40pcs / ibhokisi

2000PCS/CTN,66*36*56.5cm,18.5KG

Ixesha lokukhokhela:

Ubuninzi (amaqhekeza)	1 - 1000	1001 - 10000	>10000
Ixesha lokuhamba (iintsuku)	7	30	Kuza kuthethathethwana

Inkqubo yoVavanyo

1. Uvavanyo lweOne Step lunokwenziwa lusetyenziswe kwilindle.

2. Qokelela umyinge owaneleyo welindle (1-2 ml okanye 1-2 g) kwindawo ecocekileyo, eyomileyo yokuqokelela isampuli ukuze ufumane i-antigens ephezulu (ukuba ikhona). Iziphumo ezingcono kakhulu ziya kufumaneka ukuba iimvavanyo zenziwe kwiiyure ze-6 emva kokuqokelela.

3.Isampuli eqokelelweyo ingagcinwa iintsuku ezi-3 kwi-2-8℃ ukuba ayivavanywanga kwiiyure ezi-6. Ukugcina ixesha elide, iisampuli kufuneka zigcinwe ngaphantsi -20 ℃.

4.Khumbula i-cap ye-tube yokuqokelela i-specimen, emva koko uhlabe ngokungenamkhethe i-specimen collection applicator kwi-fecal specimen ubuncinane kwiindawo ezi-3 ezahlukeneyo ukuqokelela malunga ne-50 mg ye-feces (elingana ne-1/4 ye-pea). Musa ukukhupha i-fecal ye-membrane) ayijongwa kwifestile yovavanyo emva komzuzu omnye, yongeza enye ithontsi yesampulu kwi-specimen kakuhle.

Okuhle: kuvela imigca emibini. Umgca omnye kufuneka uhlale uvela kumgca wolawulo (C), kwaye omnye umgca ocacileyo onemibala kufuneka uvele kwindawo yovavanyo.

Okubi: Umgca omnye onemibala ubonakala kummandla wolawulo (C) .Akukho mgca wombala obonakalayo ovela kummandla wovavanyo.

Ayisebenzi: Umgca wolawulo awubonakali. Umthamo wesampulu engonelanga okanye ubuchule benkqubo obungachanekanga zezona zizathu ezinokuthi zibe kho zokungaphumeleli komgca wolawulo.

★ Hlaziya inkqubo kwaye uphinda uvavanyo ngesixhobo esitsha sovavanyo. Ukuba ingxaki iyaqhubeka, yeka ukusebenzisa ikiti yovavanyo ngoko nangoko kwaye uqhagamshelane nomsasazi wakho wendawo.

Uluhlu lweeMveliso

Igama lemveliso	Umzekelo	Ifomathi	Isatifikethi
Umkhuhlane Ag A Uvavanyo	Ngempumlo / Nasopharyngeal Swab	Ikhasethi	CE ISO
Uvavanyo lwe-Influenza Ag B	Ngempumlo / Nasopharyngeal Swab	Ikhasethi	CE ISO
HCV Hepatitis C Virus Ab Uvavanyo	WB/S/P	Ikhasethi	ISO
HIV 1+2 Test	WB/S/P	Ikhasethi	ISO
HIV 1/2 Tri-line Test	WB/S/P	Ikhasethi	ISO
HIV 1/2/O Antibody Test	WB/S/P	Ikhasethi	ISO
Uvavanyo lweDengue IgG/IgM	WB/S/P	Ikhasethi	CE ISO
Uvavanyo lweDengue NS1 Antigen	WB/S/P	Ikhasethi	CE ISO
Uvavanyo lweDengue IgG/IgM/NS1 Antigen	WB/S/P	Ikhasethi	CE ISO
Uvavanyo lwe-H.Pylori Ab	WB/S/P	Ikhasethi	CE ISO
Uvavanyo lwe-H.Pylori Ag	Ilindle	Ikhasethi	CE ISO
Uvavanyo lweSyphilis (Anti-treponemia Pallidum).	WB/S/P	Ikhasethi	CE ISO
Uvavanyo lweTyphoid IgG/IgM	WB/S/P	Ikhasethi	CE ISO
Uvavanyo lwe-Toxo IgG/IgM	WB/S/P	Ikhasethi	CE ISO
Uvavanyo lweSifo sePhepha	WB/S/P	Ikhasethi	CE ISO
Uvavanyo olukhawulezayo lwe-HBsAg	WB/S/P	Ikhasethi	ISO
Uvavanyo oluKhawulezayo lwe-HBsAb	WB/S/P	Ikhasethi	ISO
HBeAg Rapid Test	WB/S/P	Ikhasethi	ISO
Uvavanyo oluKhawulezayo lweHBeAb	WB/S/P	Ikhasethi	ISO
Uvavanyo oluKhawulezayo lwe-HBcAb	WB/S/P	Ikhasethi	ISO
Uvavanyo lweRotavirus	Ilindle	Ikhasethi	CE ISO
Uvavanyo lweAdenovirus	Ilindle	Ikhasethi	CE ISO
Uvavanyo lwe-Norovirus Antigen	Ilindle	Ikhasethi	ISO
Uvavanyo lwe-IgM ye-HAV Hepatitis A	WB/S/P	Ikhasethi	ISO
Uvavanyo lwe-HAV Hepatitis A lwe-IgG/IgM	WB/S/P	Ikhasethi	CE ISO
IMalaria Ag pf/pv Uvavanyo lomgca wesithathu	WB	Ikhasethi	CE ISO
Malaria Ag pf/pan Uvavanyo lomgca wesithathu	WB	Ikhasethi	ISO
IMalariya Ab pf/pv Uvavanyo lomgca wesithathu	WB	Ikhasethi	CE ISO
Uvavanyo lweMalariya Ag pv	WB	Ikhasethi	CE ISO
Uvavanyo lweMalariya Ag pf	WB	Ikhasethi	CE ISO
Malaria Ag pan Test	WB	Ikhasethi	CE ISO
Uvavanyo lweLeishmania IgG/IgM	ISerum/Plasma	Ikhasethi	CE ISO
Uvavanyo lweLeptospira IgG/IgM	ISerum/Plasma	Ikhasethi	CE ISO
Uvavanyo lweBrucellosis(Brucella)IgG/IgM	WB/S/P	Ikhasethi	CE ISO
Chikungunya IgM Test	WB/S/P	Ikhasethi	CE ISO
Chlamydia trachomatis Ag Test	I-Endocervical Swab / Urethral swab	Ikhasethi	ISO
Uvavanyo lweNeisseria Gonorrhoeae Ag	I-Endocervical Swab / Urethral swab	Ikhasethi	CE ISO
Uvavanyo lweChlamydia Pneumoniae Ab IgG/IgM	WB/S/P	Ikhasethi	CE ISO
Uvavanyo lweChlamydia Pneumoniae Ab IgM	WB/S/P	Ikhasethi	ISO
Uvavanyo lweMycoplasma Pneumoniae Ab IgG/IgM	WB/S/P	Ikhasethi	CE ISO
Uvavanyo lweMycoplasma Pneumoniae Ab IgM	WB/S/P	Ikhasethi	CE ISO
Uvavanyo lwe-Rubella virus ye-Ab IgG/IgM	WB/S/P	Ikhasethi	CE ISO
Cytomegalo virus Antibody IgG/IgM Test	WB/S/P	Ikhasethi	CE ISO
Herpes simplex virus Ⅰ antibody IgG/IgM test	WB/S/P	Ikhasethi	CE ISO
Herpes simplex virus Ⅱ antibody IgG/IgM test	WB/S/P	Ikhasethi	CE ISO
Uvavanyo lweZika virus antibody IgG/IgM	WB/S/P	Ikhasethi	CE ISO
Uvavanyo lwe-IgM yentsholongwane ye-Hepatitis E	WB/S/P	Ikhasethi	CE ISO
Uvavanyo lwe-Influenza Ag A + B	Ngempumlo / Nasopharyngeal Swab	Ikhasethi	CE ISO
HCV/HIV/SYP Multi Combo Test	WB/S/P	Ikhasethi	ISO
Uvavanyo lwe-MCT HBsAg/HCV/HIV Multi Combo Test	WB/S/P	Ikhasethi	ISO
Uvavanyo lwe-HBsAg/HCV/HIV/SYP Multi Combo	WB/S/P	Ikhasethi	ISO
Monkey Pox Antigen Test Cassette	I-Oropharyngeal swab	Ikhasethi	CE ISO

Iprofayile yekhampani

Thina, i-Hangzhou Testsea Biotechnology Co., Ltd yinkampani ekhula ngokukhawuleza yobuchwephesha bebhayoloji ekhethekileyo ekuphandeni, ekuphuhliseni, ekuveliseni nasekusasazeni iikhithi zovavanyo lwe-in-vitro diagnostic (IVD) kunye nezixhobo zonyango.

Indawo yethu yi-GMP, ISO9001, kunye ne-ISO13458 eqinisekisiweyo kwaye sinemvume ye-CE FDA. Ngoku sijonge phambili ekusebenzisaneni neenkampani zaphesheya kwezilwandle ngophuhliso olufanayo.

Sivelisa uvavanyo lokuchuma, uvavanyo lwezifo ezosulelayo, uvavanyo lokusetyenziswa kakubi kweziyobisi, uvavanyo lwentliziyo, uvavanyo lokumakisha ithumba, uvavanyo lokutya kunye nokhuseleko kunye novavanyo lwezifo zezilwanyana, ukongezelela, uphawu lwethu lwe-TESTSEALABS luye lwaziwa kakhulu kwiimarike zasekhaya naphesheya. Umgangatho ogqwesileyo kunye namaxabiso ancomekayo asenza sikwazi ukuthatha ngaphezulu kwe-50% yezabelo zasekhaya.

Testsea Disease Test H.pylori Ab Rapid Test Kit

Inkcazelo emfutshane:

Iinkcukacha zeMveliso

Iithegi zeMveliso

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