“西門子”C型肝炎抗體檢驗試劑組

醫材分類

• B.4020分析特定試劑

醫器規格

#03438099: 200 tests, #03439141: 2 x 7 ml negative control, 2 x 7 ml positive control

限制項目

輸 入

適應症

以三明治免疫法定性偵測人體血清或血漿中是否有C型肝炎病毒免疫球蛋白(IgG)抗體。

醫材資訊

主成分

HCV ReadyPack includes:\nSolid Phase 20.0 ml containing Streptavidin coated paramagnetic microparticles performed with biotinylated recombinated c200 HCV Ag and biotinylated synthetic c22p HCV Ag (~0.3 μg/ml) in buffer with surfactant, stabilizerd and preservatives.\nAncillary Reagent 10.0 ml containing biotinylated recombinant NS5HCV Ag (~0.5 μg/ml) in buffer with sodium azide (<0.1%) and surfactant.\nLite Reagent 10.0 ml containing anti-human IgG monoclonal Ab (~0.05 μg/ml) labeled with acridinium ester in buffer with bovine serum albumin, sodium azide (<0.1%) and surfactant.\nAncillary ReadyPack 20.0 ml containing bovine serum albumin, goat serum, sodium azide (<0.1%), surfactant.\nHCV calibrator vials 2.0 ml/vial processed human plasma negative and positive for HCV with preservatives.\nHCV quality control material containing 10.0 ml/vial processed human plasma negative and positive for Anti-HCV with preservatives.

製造商

SIEMENS HEALTHCARE DIAGNOSTICS INC.

製造國

US

申請商

西門子醫療設備股份有限公司

有效日期

2030/02/02

發證日期

2010/02/02

供應藥局

目前尚無登錄供應此品項的藥局資料。