“西門子”人類免疫不全病毒1/O/2型加強試驗組

醫材分類

• B.4020分析特定試劑

醫器規格

#01463908:200 tests, #01324827:2x7.0ml Negative control, 2x7.0ml positive control 1, 2x7.0 ml positive control 2.

限制項目

輸 入

適應症

利用ADVIA Centaur®及ADVIA Centaur XP System發展之免疫法在體外定性偵測血清或血漿中的抗人類免疫不全病毒第一型及其O亞型抗體，與第二型抗體。

醫材資訊

主成分

(1)Solid Phase 20.0 ml containing Streptavidin-coated paramagnetic microparticles preformed with biotinylated HIV antigens (~1.0μg/mL) in buffer with bovine serum albumin, goat serum, surfactant, and preservatives.\n(2)Lite Reagent 10.0 ml containing recombinant HIV antigens, labeled with acridinium ester in buffer with bovine serum albumin, mouse lgG, goat serum, surfactant, and preservatives.\n(3)Ancillary Lite Reagent 10.0 ml containing recombinant HIV antigens labeled with acridinium ester in buffer with bovine serum albumin, mouse lgG, goat serum, surfactant, and preservatives.\n(4)EHIV calibrator vials: 2.0 ml/vial processed human plasma negative for antibodies toHIV spiked with antibodies to HIV-1, sodium azide (<0.1%) and preservatives.\n\nEHIV quality control material containing 7.0 ml/vial processed human plasma nonreactive for HIV, reactive for HIV-1, and reactive for HIV-2 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

2029/07/27

發證日期

2009/07/27

供應藥局

目前尚無登錄供應此品項的藥局資料。