Uvavanyo lweSifo seTestsea TOXO IgG/IgM Rapid Test Kit
Iinkcukacha eziKhawulezayo
Igama lebrand: | Testsea | Igama lemveliso: | TOXO IgG/IgM Rapid Test Kit |
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/Strip | 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
Inkqubo yoVavanyo
Vumela uvavanyo, umfuziselo, isithinteli kunye/okanye ulawulo lufikelele kubushushu begumbi 15-30℃ (59-86℉) phambi kovavanyo.
1. Zisa isingxobo kwiqondo lobushushu begumbi phambi kokuba usivule. Susa isixhobo sovavanyo kwisingxobo esivaliweyo kwaye usisebenzise ngokukhawuleza.
2. Beka isixhobo sokuvavanya kwindawo ecocekileyo kunye nenqanaba.
3. Kwi-serum okanye isampuli yeplasma: Bamba idropha ngokuthe nkqo kwaye udlulisele amathontsi ama-3 e-serum okanye iplasma (malunga ne-100μl) kumzekelo wequla (S) lesixhobo sovavanyo, emva koko uqalise isibali-xesha. Jonga umfanekiso ongezantsi.
4. Kwimizekelo yegazi elipheleleyo: Bamba i-dropper ngokuthe nkqo kwaye udlulisele i-1 ithontsi legazi elipheleleyo (malunga ne-35μl) kwi-specimen well(S) yesixhobo sovavanyo, uze udibanise ama-2 amathontsi e-buffer (malunga ne-70μl) kwaye uqalise isibali-xesha. Jonga umfanekiso ongezantsi.
5. Lindela ukuba kuvele umgca onemibala. Funda iziphumo ngemizuzu eyi-15. Musa ukutolika umphumo emva kwemizuzu engama-20.
Ukusebenzisa isixa esaneleyo somzekelo kubalulekile kwisiphumo sovavanyo esisebenzayo. Ukuba ukufuduka (ukumanzisa kwenwebu) akujongwa kwifestile yovavanyo emva komzuzu omnye, yongeza ithontsi elinye ngaphezulu le-buffer (yegazi elipheleleyo) okanye isampuli (yeserum okanye iplasma) kumzekelo kakuhle.
Ukutolikwa kweziPhumo
Okuhle:Kuvela imigca emibini. Umgca omnye kufuneka uhlale uvela kumgca wolawulo (C), kwaye omnye umgca ocacileyo onemibala kufuneka uvele kwindawo yovavanyo.
Engalunganga:Umgca omnye onemibala ubonakala kummandla wokulawula (C) .Akukho mgca wembala obonakalayo ovela kummandla wovavanyo.
Ayisebenzi:Umgca wolawulo uyasilela ukubonakala. 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.