適應症
利用放射性免疫定量方法檢測血清或血漿中的睪丸脂酮荷爾蒙。  
劑型
 
包裝
DSL-4000: 100 tubesDSL-4000-5: 500 tubes 
許可證字號
衛部藥製字第015907號 
註銷狀態
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
常盈睪丸脂酮檢驗試劑 
英文品名
DSL Testosterone CT RIA 
藥品類別
A 臨床化學及臨床毒理學 
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
DHAS0601590700 
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 C-peptide Standards: One vial, labeled A, containing 0 ng/mL, and five vials, labeled B-F, containing approximate concentrations of 0.1, 0.5, 1.5, 5 and 20 ng/mL (0.033-6.66 nmol/L) of C-peptide in a protein-based buffer with sodium azide as a preservative.C-peptide [I-125] Reagent: One vial containing < 5 μCi (185 kBq) of [I-125]-labeled C-peptide in a protein-based buffer with sodium azide as a preservative.C-peptide Antiserum: One vial containing guinea pig anti-C-peptide serum in a protein-based buffer with sodium azide as a preservative.Precipitating Reagent: One bottle, 105 mL, containing goat anti-guinea pig gamma globulin serum in a buffered solution with polyethylene glycol as a precipitating aid and sodium azide as a preservative.C-peptide Controls: Two vials, Levels I and II, containing a low and high level of C-peptide with sodium azide as a preservative.