Qizhe α fetoprotein in vitro reagent group - Taiwan Registration 720b2528f34b14c11c10e47299d90308
Access comprehensive regulatory information for Qizhe α fetoprotein in vitro reagent group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 720b2528f34b14c11c10e47299d90308 and manufactured by Longteng Biotechnology Co., Ltd. The authorized representative in Taiwan is Qizhe Biotechnology Co., Ltd.
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Device Details
Product Details
Qualitative detection of AFP in human serum.
C Immunology and microbiology
C.6010 腫瘤相關抗原免疫試驗系統
Contract manufacturing;; Domestic
Dates and Status
Dec 11, 2013
Dec 07, 2016
Apr 25, 2018
Cancellation Information
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