510(k) Premarket Notification | 合法醫療器材資訊網
DeviceClassificationName,test,time,prothrombin22.510(k)Number,K013155.DeviceName,DADETHROMBOPLASTINCPLUS.Applicant ...
References Products Classification Database Information for Test, Time, Prothrombin (www.accessdata.fda.gov) Code of Federal Regulations (CFR) database information for 864.7750 (www.accessdata.fda.gov) PDF for K013155 (www.accessdata.fda.gov) Device Classification Name test, time, prothrombin[1] 510(k) Number K013155 Device Name DADE THROMBOPLASTIN C PLUS Applicant DADE BEHRIN...
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510(k) Premarket Notification | 合法醫療器材資訊網
Device Classification Name, test, time, prothrombin22. 510(k) Number, K013155. Device Name, DADE THROMBOPLASTIN C PLUS. Applicant ... Read More
BCS XP System | 合法醫療器材資訊網
Factor VII-Dade Innovin Factor VII-Dade Thromboplastin C Plus Factor VII-Thromborel S Factor VIII-Dade Actin Factor VIII-Dade Actin FS Factor VIII-Dade Actin ... Read More
K964139.pdf | 合法醫療器材資訊網
1997年2月6日 — (Dade® Innovin®, INR). Derived Fibrinogen. (Dade® Innovin®). Prothrombin Time. (Dade® Thromboplastin C Plus, seconds). Prothrombin ... Read More
K981711.pdf | 合法醫療器材資訊網
1998年9月30日 — Dade Behring Inc. 1851 Delaware ... (Dade® Thromboplastin C Plus,seconds). 104. 0.983 ... Activated Partial Thromboplastin Time. (Dade® ... Read More
THROMBOPLASTIN C PLUS REAGENT * Adverse Event ... | 合法醫療器材資訊網
... medical devices. This maude entry was filed with the FDA on 2006-09-22 for THROMBOPLASTIN C PLUS REAGENT * manufactured by Dade-behring. Read More
US5625036A | 合法醫療器材資訊網
1998-06-08 Assigned to DADE BEHRING INC. reassignment DADE ... The Dade® thromboplastin reagents, Thromboplastin C, C+, and IS, are all based on ... Read More
戴德凝血活酶C+ 凝血酶原試劑DADE THROMBOPLASTIN C PLUS ... | 合法醫療器材資訊網
戴德凝血活酶C+ 凝血酶原試劑DADE THROMBOPLASTIN C PLUS / 測定PT(PROTHROMBIN TIME)以及其他需要PT的血液凝固測試。 / 藥要看提供簡單的介面 ... Read More
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【戴德凝血活酶 C+ 凝血酶原試劑】許可證字號:衛署醫器輸字第012214號
器材品名:戴德凝血活酶C+凝血酶原試劑許可證字號:衛署醫器輸字第012214號註銷狀態:已註銷註銷日期:2013/01/21註銷理由:許可...