Uvavanyo lweSyphilis yeSifo seTestsea (Anti-treponemia Pallidum) Uvavanyo
Iinkcukacha eziKhawulezayo
| Igama lebrand: | Testsea | Igama lemveliso: | Uvavanyo lweSyphilis (Anti-treponemia Pallidum). |
| 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 |
Inkcazo yevidiyo
Ukusetyenziswa okucetywayo
I-Syphilis (SYP) i-Antibody Rapid Test Cassette (Igazi Elipheleleyo/iSerum/Plasma) luvavanyo olukhawulezayo, lwe-serological, lwe-immunochromatographic lokufumanisa umgangatho we-antibodies (IgG, IgM kunye ne-IgA) ukuya kwi-Treponema Pallidum (TP) kwi-serum yabantu okanye iplasma. Kujongwe ukuba kusetyenziswe uvavanyo lokuhlola kwaye njengoncedo ekuxilongeni usulelo nge-TP. Nawuphi na umzekelo osebenzayo kunye ne-SYP Ab Rapid Test Cassette kufuneka uqinisekiswe ngenye indlela yovavanyo kunye neziphumo zekliniki.
Isishwankathelo
I-Treponema Pallidum (TP) yi-agent e-causative ye-syphilis yesifo se-venereal. I-TP yintsholongwane ye-spirochete enemvulophu yangaphandle kunye ne-membrane ye-cytoplasmic. Kuncinci okwaziwayo malunga nomzimba xa kuthelekiswa nezinye iintsholongwane zebhaktiriya. Ngokutsho kweZiko Lolawulo Lwezifo (CDC), inani leemeko zosulelo lwegcushuwa liye landa ngokuphawulekayo ukususela ngowe-1985. Abanye oothunywashe abaphambili abaye bafak’ isandla koku kwanda baquka ubhubhani we<em>crack nokwanda kobuhenyu phakathi kwabantu abasebenzisa iziyobisi. Olunye uphononongo luxele ukuba inani elikhulu labasetyhini abosulelwe yi-HIV babonise iziphumo zovavanyo lwe-syphilis esebenzayo. Izigaba ezininzi zeklinikhi kunye nexesha elide losulelo olufihlakeleyo, olungenazimpawu luphawu lwegcushuwa. Usulelo lwe-syphilis olusisiseko luchazwa kubukho be-chancre kwindawo yokugonywa. Impendulo ye-antibody kwibhaktheriya ye-TP inokubonwa phakathi kweentsuku ezi-4 ukuya kwezi-7 emva kokuvela kwe-chancre. Usulelo luhlala lubonakala de isigulane sifumane unyango olwaneleyo.
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 |
Iimveliso ezinxulumeneyo
Ulwazi Lomboniso
Isatifikethi sembeko
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.
OUKUPAKISHA & UKUTHUMELA
FAQ
Sizinze eZhejiang, eChina, siqale ngo-2015, sithengisela uMzantsi-mpuma Asia (15.00%), iMarike yasekhaya (15.00%), eMzantsi, eMelika (10.00%), eAfrika (10.00%), eMntla Melika (5.00%), eMpuma
IYurophu(5.00%), i-Oceania(5.00%), uMbindi Mpuma(5.00%),eMpuma Asia(5.00%),iNtshona Yurophu(5.00%),uMbindi Merika(5.00%), uMntla Yurophu(5.00%),uMzantsi Yurophu( 5.00%),South Asia(5.00%). Kukho abantu abamalunga nama-51-100 eofisini yethu.
Ngalo lonke ixesha isampuli yangaphambi kokuveliswa phambi kwemveliso yobuninzi;
Ukuhlolwa kokugqibela rhoqo ngaphambi kokuthunyelwa;
Uvavanyo oluKhawulezayo lwezilwanyana, iiKhithi zoVavanyo lokuchuma, iiKhithi zoVavanyo lweSiyobisi, iiKhithi zoVavanyo lweSifo esosulelayo, uVavanyo lwaMakishi eTumor, uvavanyo loKhuseleko lokutya
Amandla atyebileyo kwitekhnoloji, izixhobo eziphambili, inkqubo yolawulo lwangoku, uluhlu olubanzi lweekhithi zovavanyo olukhawulezayo lweklinikhi, usapho kunye nokuxilongwa kwelebhu, ISO, CE FSC eqinisekisiweyo.
IMigaqo yokuhanjiswa eyamkelweyo: FOB, CIF, EXW, FCA, DDP, ukuhanjiswa kweExpress;
Imali eyamkelekileyo yeNtlawulo: USD;RMB
Uhlobo lweNtlawulo olwamkelweyo: T/T, Western Union,Escrow;
Ulwimi oluthethwayo: IsiNgesi