I-Testsea Disease Test H.pylori Ab Rapid Test Kit
Imininingwane Esheshayo
| I gama le-brand: | I-Testsea | Igama lomkhiqizo: | Ukuhlolwa kwe-H.Pylori Ab |
| Indawo Yomsuka: | I-Zhejiang, China | Uhlobo: | Izinsiza Zokuhlaziya I-Pathological |
| Isitifiketi: | CE/ISO9001/ISO13485 | Ukuhlukaniswa kwezinsimbi | Ikilasi III |
| Ukunemba: | 99.6% | Isifanekiso: | Igazi Eliphelele/iSerum/Plasma |
| Ifomethi: | Ikhasethi | Ukucaciswa: | 3.00mm/4.00mm |
| I-MOQ: | 1000 Pcs | Impilo yeshelufu: | iminyaka engu-2 |
| OEM & ODM | ukusekela | Ukucaciswa: | 40pcs/ibhokisi |
Supply Amandla:
5000000 Ucezu/Izingcezu Ngenyanga
Ukupakisha nokulethwa:
Imininingwane yokupakisha
40pcs/ibhokisi
2000PCS/CTN, 66*36*56.5cm, 18.5KG
Isikhathi esiholayo:
| Ubuningi(izingcezu) | 1 - 1000 | 1001 - 10000 | > 10000 |
| Isikhathi sokuhola (izinsuku) | 7 | 30 | Kuzoxoxiswana |
Inqubo Yokuhlola
1. I-One Step Test ingenziwa isetshenziswe endle.
2. Qoqa inani elanele lendle (1-2 ml noma 1-2 g) esitsheni esihlanzekile, esomile seqoqo lesampula ukuze uthole ama-antigen aphezulu (uma ekhona). Imiphumela emihle kakhulu izotholakala uma ukuhlolwa kwenziwe phakathi namahora angu-6 ngemva kokuqoqwa.
3.Isifanekiso esiqoqiwe singagcinwa izinsuku ezi-3 ku-2-8℃ uma singahloliwe phakathi kwamahora angu-6. Ukugcina isikhathi eside, ama-specimens kufanele agcinwe ngaphansi -20 ℃.
4.Khumula isikulufu seshubhu lokuqoqwa kwesampula, bese ugwaza ngokungahleliwe isisetshenziswa esiqoqiwe sesampula endaweni ye-fecal okungenani ezindaweni ezi-3 ezihlukene ukuze uqoqe cishe u-50 mg wendle (okulingana ne-1/4 yephizi). Ungayikhiphi i-fecal ye-membrane) ayibonwa efasiteleni lokuhlola ngemva komzuzu owodwa, engeza ithonsi elilodwa lesampula emthonjeni kahle.
Okuhle: Kuvela imigqa emibili. Umugqa owodwa kufanele uvele njalo endaweni yomugqa wokulawula(C), futhi omunye ulayini obonakalayo onombala kufanele uvele endaweni yomugqa wokuhlola.
Okubi: Umugqa owodwa onombala uvela endaweni yokulawula(C).Awukho umugqa onombala obonakalayo ovela endaweni yomugqa wokuhlola.
Akuvumelekile: Ulayini wokulawula uyehluleka ukuvela. Ivolumu yesampula enganele noma izindlela zenqubo ezingalungile yizona zizathu okungenzeka kakhulu zokwehluleka komugqa wokulawula.
★ Buyekeza inqubo bese uphinda ukuhlolwa ngedivayisi entsha yokuhlola. Uma inkinga iqhubeka, yeka ukusebenzisa ikhithi yokuhlola ngokushesha futhi uxhumane nomsabalalisi wangakini.
Uhlu Lomkhiqizo
| Igama lomkhiqizo | Isifanekiso | Ifomethi | Isitifiketi |
| I-Influenza Ag A Test | I-Nasopharyngeal Swab | Ikhasethi | CE ISO |
| Ukuhlolwa komkhuhlane we-Ag B | I-Nasopharyngeal Swab | Ikhasethi | CE ISO |
| I-HCV Hepatitis C Virus Ab Test | I-WB/S/P | Ikhasethi | ISO |
| I-HIV 1+2 Test | I-WB/S/P | Ikhasethi | ISO |
| HIV 1/2 Tri-line Test | I-WB/S/P | Ikhasethi | ISO |
| Ukuhlolwa kwe-HIV 1/2/O Amasosha omzimba | I-WB/S/P | Ikhasethi | ISO |
| Ukuhlolwa kweDengue IgG/IgM | I-WB/S/P | Ikhasethi | CE ISO |
| Ukuhlolwa kwe-Dengue NS1 Antigen | I-WB/S/P | Ikhasethi | CE ISO |
| Ukuhlolwa kwe-Dengue IgG/IgM/NS1 Antigen | I-WB/S/P | Ikhasethi | CE ISO |
| Ukuhlolwa kwe-H.Pylori Ab | I-WB/S/P | Ikhasethi | CE ISO |
| Ukuhlolwa kwe-H.Pylori Ag | Indle | Ikhasethi | CE ISO |
| I-Syphilis (Anti-treponemia Pallidum) Ukuhlolwa | I-WB/S/P | Ikhasethi | CE ISO |
| Ukuhlolwa kweTyphoid IgG/IgM | I-WB/S/P | Ikhasethi | CE ISO |
| Ukuhlolwa kwe-Toxo IgG/IgM | I-WB/S/P | Ikhasethi | CE ISO |
| Ukuhlolwa Kwesifo Sofuba | I-WB/S/P | Ikhasethi | CE ISO |
| Ukuhlolwa Okusheshayo kwe-HBsAg | I-WB/S/P | Ikhasethi | ISO |
| Ukuhlolwa Okusheshayo kwe-HBsAb | I-WB/S/P | Ikhasethi | ISO |
| Isivivinyo Esisheshayo se-HBeAg | I-WB/S/P | Ikhasethi | ISO |
| Isivivinyo Esisheshayo se-HBeAb | I-WB/S/P | Ikhasethi | ISO |
| Ukuhlolwa Okusheshayo kwe-HBcAb | I-WB/S/P | Ikhasethi | ISO |
| Ukuhlolwa kwe-Rotavirus | Indle | Ikhasethi | CE ISO |
| Ukuhlolwa kwe-Adenovirus | Indle | Ikhasethi | CE ISO |
| Ukuhlolwa kwe-Norovirus Antigen | Indle | Ikhasethi | ISO |
| I-HAV Hepatitis A virus Test IgM | I-WB/S/P | Ikhasethi | ISO |
| I-HAV Hepatitis A virus Test IgG/IgM | I-WB/S/P | Ikhasethi | CE ISO |
| I-Malaria Ag pf/pv Ukuhlolwa kwe-Tri-line | WB | Ikhasethi | CE ISO |
| I-Malaria Ag pf/pan Tri-line Test | WB | Ikhasethi | ISO |
| Umalaleveva Ab pf/pv Ukuhlolwa Kwemigqa Emithathu | WB | Ikhasethi | CE ISO |
| I-Malaria Ag pv Test | WB | Ikhasethi | CE ISO |
| I-Malaria Ag pf Test | WB | Ikhasethi | CE ISO |
| Umalaleveva Ag pan Test | WB | Ikhasethi | CE ISO |
| Ukuhlolwa kwe-Leishmania IgG/IgM | ISerum/Plasma | Ikhasethi | CE ISO |
| Ukuhlolwa kwe-Leptospira IgG/IgM | ISerum/Plasma | Ikhasethi | CE ISO |
| Ukuhlolwa kwe-Brucellosis(Brucella)IgG/IgM | I-WB/S/P | Ikhasethi | CE ISO |
| Chikungunya IgM Test | I-WB/S/P | Ikhasethi | CE ISO |
| Ukuhlolwa kwe-Chlamydia trachomatis Ag | I-Endocervical Swab/Urethral swab | Ikhasethi | ISO |
| Ukuhlolwa kwe-Neisseria Gonorrhoeae Ag | I-Endocervical Swab/Urethral swab | Ikhasethi | CE ISO |
| I-Chlamydia Pneumoniae Ab IgG/IgM Test | I-WB/S/P | Ikhasethi | CE ISO |
| I-Chlamydia Pneumoniae Ab IgM Test | I-WB/S/P | Ikhasethi | ISO |
| I-Mycoplasma Pneumoniae Ab IgG/IgM Test | I-WB/S/P | Ikhasethi | CE ISO |
| I-Mycoplasma Pneumoniae Ab IgM Test | I-WB/S/P | Ikhasethi | CE ISO |
| I-Rubella virus Test Ab IgG/IgM | I-WB/S/P | Ikhasethi | CE ISO |
| Ukuhlolwa kwe-Cytomegalo virus Antibody IgG/IgM | I-WB/S/P | Ikhasethi | CE ISO |
| I-Herpes simplex virus Ⅰ ukuhlolwa kwe-antibody IgG/IgM | I-WB/S/P | Ikhasethi | CE ISO |
| I-Herpes simplex virus Ⅱ i-antibody IgG/IgM test | I-WB/S/P | Ikhasethi | CE ISO |
| Ukuhlolwa kwe-Zika virus antibody IgG/IgM | I-WB/S/P | Ikhasethi | CE ISO |
| Ukuhlolwa kwe-Hepatitis E virus antibody IgM | I-WB/S/P | Ikhasethi | CE ISO |
| Ukuhlolwa komkhuhlane we-Ag A+B | I-Nasopharyngeal Swab | Ikhasethi | CE ISO |
| I-HCV/HIV/SYP Multi Combo Test | I-WB/S/P | Ikhasethi | ISO |
| I-MCT HBsAg/HCV/HIV Multi Combo Test | I-WB/S/P | Ikhasethi | ISO |
| I-HBsAg/HCV/HIV/SYP Multi Combo Test | I-WB/S/P | Ikhasethi | ISO |
| Ikhasethi Lokuhlola I-Monkey Pox Antigen | I-Oropharyngeal swab | Ikhasethi | CE ISO |
Iphrofayela Yenkampani
Thina, i-Hangzhou Testsea Biotechnology Co., Ltd yinkampani ekhula ngokushesha yobuchwephesha be-biotechnology ekhethekile ekucwaningeni, ekuthuthukiseni, ekukhiqizeni nasekusabalaliseni amakhithi okuhlola e-in-vitro diagnostic(IVD) athuthukile namathuluzi ezokwelapha.
Indawo yethu yi-GMP, ISO9001, kanye ne-ISO13458 futhi sinemvume ye-CE FDA. Manje sesibheke ngabomvu ukubambisana nezinye izinkampani zaphesheya ukuze sithuthukiselane.
Sikhiqiza ukuhlolwa kwenzalo, ukuhlolwa kwezifo ezithathelwanayo, ukuhlola ukusetshenziswa kabi kwezidakamizwa, ukuhlola umaka wenhliziyo, ukuhlolwa komaka isimila, ukuhlolwa kokudla nokuphepha kanye nokuhlolwa kwezifo zezilwane, ngaphezu kwalokho, uhlobo lwethu lwe-TESTSEALABS lwaziwa kakhulu ezimakethe zasekhaya neziphesheya kwezilwandle. Izinga eliphezulu nezintengo ezivumayo zisenza sikwazi ukuthatha amasheya asekhaya angaphezu kuka-50%.