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⚠️ 此醫材許可證已註銷

狀態:已註銷 日期:2012/11/27

原因:許可證已逾有效期

"代首林" 副甲狀腺激素放射免疫分析試劑

🩺 醫材

"DiaSorin" N-tact PTH SP

衛署醫器輸字第015421號

GDP 認證供應商

醫材分類

  • A.1545副甲狀腺激素試驗系統

醫器規格

#26100: 100 tests

限制項目

輸入須附同意書(每次輸入均須取得原子能委員會之同意書為憑);;輸 入

適應症

定量檢測人體血清或血漿中生物活性之原態副甲狀腺素(hPTH 1-84)之含量。

醫材資訊

主成分
1.N-tact PTH SP Calibrator 0: 1 vial 15 mL. Contains human serum with 0.1% sodium azide added as a preservative.2.N-tact PTH SP Calibrator 1-5:lyophilyzed reagent. Set of 5 human PTH 1-84 calibrators, at nominal concentrations ranging from 15-2000 pg/mL, contains 0.1% sodium azide and other stabilizers.3.N-tact PTH SP Beads: 1 container, 100 beads. Polystyrene beads are coated with affinity-purified goat antibody specific for the 39-84 sequence of PTH.4.I-125 N-tact PTH SP Antibody: 2 vials. Each vial contains 5.0 mL of affinity purified goat antibody specific for PTH 1-34, labeled with iodine-125. 5.N-tact PTH SP Wash Solution Concentrate. 1 vial, 50 mL.Contains a concentrated buffered surfactant. Prepare a working wash solution by diluting the entire vial contents with 450 mL of distilled or deionized water. 6. N-tact PTH SP Control, Level 1 and Level 2:2 vials lyophilized reagent. Human serum is spiked with hPTH 1-84 to obtain a concentration with a specified range. 0.1% sodium azide is added.
製造商
DIASORIN INC.
製造國
US
申請商
泰歷藥品儀器股份有限公司
有效日期
2010/12/10
發證日期
2005/12/10

供應藥局

目前尚無登錄供應此品項的藥局資料。