貝克曼庫爾特亞瑟斯茶鹼試劑

BECKMAN COULTER Access Theophylline Reagent

衛署醫器輸字第012290號

本站收錄狀態已註銷

有效日期2010 / 09 / 12

醫療器材級數未載明

這張許可證已註銷（2011/02/17，自請註銷），以下僅供查閱歷史資料。申請商為 美商貝克曼庫爾特有限公司台灣分公司。以下整理許可證、規格與製造廠資料，供核對產品身分使用。

許可證資料依公開資料欄位整理

效能: 定量偵測人類血清中茶鹼的量。
規格: 亞瑟斯茶鹼試劑: 2×50Tests/Kit亞瑟斯茶鹼校正液: 6×4.0 mL
主成分: Access Theophylline ReagentR1a: Paramagnetic particles coated with goat anti-mouse IgG suspended in TRIS buffered saline, with surfactant, bovine serum albumin (BSA) matrix, <0.1% sodium azide, and 0.1% ProClin** 300. R1b: Theophylline-alkaline phosphatase (bovine) conjugate diluted in TRIS buffered saline, with surfactant, BSA matrix, <0.1% sodium azide, and 0.25% ProClin 300. R1c: Mouse monoclonal antibody to theophylline diluted in TRIS buffered saline, with surfactant, BSA matrix, <0.1% sodium azide, and 0.1% ProClin 300. Access Theophylline CalibratorsS0: Human serum with <0.1% sodium azide, and 0.5% ProClin** 300. Contains 0.0μg/mL (μmol/L) theophylline.S1, S2, S3, S4, S5: Theophylline in human serum at levels of approximately 5.0, 10.0, 15.0, 20.0, and 40.0μg/mL (28, 56, 83, 111, and 222μmol/L), respectively, with <0.1% sodium azide, and 0.5% ProClin 300.

可改用包裝上的完整型號或許可證字號查詢。