常盈紅血球生成素分析試劑
DSL EPO RIA

適應症
利用放射性免疫定量方法檢測血清或血漿中的紅血球生成素。  
劑型
 
包裝
DSL-1100: 100 tubes 
許可證字號
衛部藥製字第015906號 
註銷狀態
1 
註銷日期
2012-11-26  
註銷理由
838 
有效日期
2011-01-17  
發證日期
2006-01-17  
許可證種類
09 
中文品名
常盈紅血球生成素分析試劑 
英文品名
DSL EPO RIA 
藥品類別
B 血液學及病理學裝置 
申請商名稱
常盈實業股份有限公司  
申請商地址
台北市北投區永興路一段49號 
通關簽審文件編號
DHAS0601590608 
資料更新時間
 
製造商
名稱 廠址 公司地址 國別 製程
DIAGNOSTIC SYSTEMS LABORATORIES, INC. 445 MEDICAL CENTER BOULEVARD WEBSTER, TEXAS 77598 U.S.A. US
成份表
處方標示 成分名稱 含量 單位
1 EPO Standards: One vial, 5 mL, labeled A, containing of 0 mIU/mL human EPO and six vials, 1 mL each, labeled B-G, containing concentrations of approximately 5, 10, 25, 50, 100 and 200 mIU/mL human EPO in a protein-based buffer with sodium azide as a preservative.EPO [I-125] Reagent: One vial, 11 mL, containing < 5 μCi (185 kBq) of [I-125]-labeled EPO in a protein-based buffer with sodium azide as a preservative. EPO Antiserum: One vial, containing rabbit anti-human EPO serum in a protein-based buffer with sodium azide as a preservative.Precipitating Reagent: One bottle, 100 mL, containing goat anti-rabbit gamma globulin serum in a buffer with polyethylene glycol as a precipitating aid and sodium azide as a preservative.EPO Controls: Two vials, 1 mL each, containing low and high concentrations of human EPO in a protein-based buffer with sodium azide as a preservative.