Testsea Chirwere Chiedza HBsAg Rapid Test Kit

Tsanangudzo Pfupi:

HBsAg Muedzo ndeyekukurumidza kuongororwa bvunzo yekuona Hepatitis B pamusoro antigen (HBsAg) muropa, serum, kana plasma. Muedzo uyu unobatsira kuona hutachiona hweHepatitis B huripo, sezvo HBsAg iri mucherechedzo unoratidza kuvepo kweutachiona hweHepatitis B (HBV).


Product Detail

Product Tags

Quick Details

Zita reBrand:

Testsea

Product name:

HBsAg Rapid Test

Nzvimbo Yekwakabva:

Zhejiang, China

Type:

Pathological Analysis Equipments

Chitupa:

ISO9001/ISO13485

Instrument classification

Kirasi III

Kururama:

99.6%

Muenzaniso:

Ropa Rakazara/Serum/Plasma

Format:

Cassette

Tsanangudzo:

3.00mm/4.00mm

MOQ:

1000 Pcs

Sherufu hupenyu:

2 years

OEM & ODM

rutsigiro

Tsanangudzo:

40pcs/bhokisi

Supply Ability:

5000000 Piece/Zvimedu pamwedzi

Packaging & delivery:

Packaging Details

40pcs/bhokisi

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

Nguva yekufambisa:

Huwandu (zvidimbu) 1 - 1000 1001 - 10000 >10000
Nguva yekufambisa (mazuva) 7 30 Kutaurirana

 

Chinangwa Kushandiswa

Iyo Imwe Nhanho HBsAg Muedzo ndeyekukurumidza chromatographic immunoassay yekuonekwa kwemhando yeHepatitis B pamusoro Antigen (HBsAg) muRopa Rakazara / Serum / Plasma.

hbs (5)
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hbs (4)

Summary

Hepatitis B inokonzerwa nehutachiona hunobata chiropa. Vanhu vakuru vanobatwa nehepatitis B vanowanzopora. Zvakadaro vacheche vazhinji vanotapukirwa pakuzvarwa vanova vatakuri vasingaperi kureva kuti vanotakura utachiona kwemakore akawanda uye vanogona kutapurira utachiona kune vamwe. Kuvapo kweHBsAg muRopa Rakazara / Serum / Plasma chiratidzo chekushanda kwehutachiona hweHepatitis B.

Test Procedure

1. The One Step Test inogona kuitwa kushandiswa patsvina.

2. Unganidza huwandu hwakakwana hwetsvina (1-2 ml kana 1-2 g) mumudziyo wakachena, wakaoma wemuenzaniso wekuunganidza kuti uwane maantigen akawanda (kana aripo). Mhedzisiro yakanakisa ichawanikwa kana ma assays akaitwa mukati meawa 6 mushure mekuunganidzwa.

3.Specimen yakaunganidzwa inogona kuchengetwa kwemazuva 3 pa 2-8 ℃ kana isina kuongororwa mukati maawa matanhatu. Nekuchengetedza kwenguva refu, zvienzaniso zvinofanirwa kuchengetwa pazasi -20 ℃.

4.Bvisa chivharo chechubhu yekuunganidza, wobva wabaya mutsara wekuunganidza wemuenzaniso mune fecal specimen munzvimbo dzinenge 3 dzakasiyana kuti utore inenge 50 mg yetsvina (yakaenzana ne1/4 yepea). Usatora fecal ye membrane) haina kucherechedzwa muhwindo rekuyedza mushure meminiti imwe, wedzera rimwe donhwe remuenzaniso kune sampuli zvakanaka.

Positive: Mitsetse miviri inooneka. Mutsetse mumwe unofanirwa kugara uchionekwa munharaunda yekudzora mutsara (C), uye imwe mutsara unoonekera weruvara unofanirwa kuoneka munharaunda yebvunzo.

Negative: Mutsara mumwe weruvara unoonekwa munzvimbo yekudzora (C) .Hapana mutsara weruvara unoonekwa munharaunda yebvunzo.

Haisiyo: Mutsetse wekudzora watadza kuoneka. Kusakwana specimen vhoriyamu kana zvisirizvo maitiro emaitiro ndizvo zvinonyanya zvikonzero zvekutadza kwekudzora mutsara.

★ Ongorora maitiro uye dzokorora bvunzo nemudziyo mutsva wekuyedza. Kana dambudziko rikaramba riripo, regedza kushandisa test kit nekukasira uye ubate mushambadzi wenzvimbo yako.

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Hepatitis E virus antibody IgM bvunzo

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Furuwenza Ag A+B Muedzo

Nasal/Nasopharyngeal Swab

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HCV/HIV/SYP Multi Combo Test

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MCT HBsAg/HCV/HIV Multi Combo Test

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Isu, Hangzhou Testsea Biotechnology Co., Ltd ikambani inokura nekukurumidza nyanzvi yebiotechnology nyanzvi mukutsvagisa, kugadzira, kugadzira uye kugovera epamberi in-vitro diagnostic (IVD) bvunzo kits uye zviridzwa zvekurapa.

Nzvimbo yedu ndeye GMP, ISO9001, uye ISO13458 certified uye isu tine CE FDA mvumo. Ikozvino tave kutarisira kushanda pamwe nemamwe makambani ari mhiri kwemakungwa mukusimudzirana.

Isu tinogadzira bvunzo dzekubereka, bvunzo dzezvirwere zvinotapukira, bvunzo dzekushandisa zvinodhaka, bvunzo dzemwoyo, bvunzo dze tumor marker, chikafu uye chengetedzo bvunzo uye bvunzo dzechirwere chemhuka, uyezve, mhando yedu TESTSEALABS yave ichizivikanwa mumisika yemumba neyekunze. Yakanakisa mhando uye mitengo yakanaka inoita kuti titore pamusoro pe50% migove yemumba.

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FAQ

1. ndisu vanaani?

Isu tinogara muZhejiang, China, kutanga kubva 2015, kutengesa kuSoutheast Asia (15.00%), Domestic Market (15.00%), South, America (10.00%), Africa (10.00%), North America (5.00%), Eastern

Europe(5.00%),Oceania(5.00%),Mid East(5.00%),Eastern Asia(5.00%),Western Europe(5.00%),Central America(5.00%),Northern Europe(5.00%),Southern Europe( 5.00%), South Asia (5.00%). Kune vanhu vanenge 51-100 muhofisi yedu.

2. tinogona sei kuvimbisa kunaka?

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Nguva dzose yekupedzisira Kuongorora kusati kwatumirwa;

3. chii chaungatenga kwatiri?

Mhuka Diagnostic Rapid Test, Fertility Test Kits, Drug of Abuse Test Kits, Infectious Disease Test Kits, Tumor Markers Test, Food Safety Test.

4. sei uchifanira kutenga kubva kwatiri, kwete kubva kune vamwe vatengesi?

Simba rakapfuma mutekinoroji, midziyo yepamberi, yemazuva ano manejimendi system, yakazara yakazara yekukurumidza bvunzo kits yekiriniki, mhuri uye yekuongorora lab, ISO, CE FSC yakasimbiswa.

5. Ndeapi mabasa atinogona kupa?

Mitemo Yekutumira Inogamuchirwa: FOB, CIF, EXW, FCA, DDP, Express Delivery;

Mari Yekubhadhara Inogamuchirwa: USD;RMB

Rudzi rweKubhadhara Yakagamuchirwa: T / T, Western Union, Escrow;

Mutauro unotaurwa: Chirungu

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