BeneCheck β-Ketone Control Solution (Non-Sterile) - Taiwan Registration f611dcc9351258d9dc80138938897bef
Access comprehensive regulatory information for BeneCheck β-Ketone Control Solution (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f611dcc9351258d9dc80138938897bef and manufactured by Qinli Biotechnology Co., Ltd. new tree factory. The authorized representative in Taiwan is GENERAL LIFE BIOTECHNOLOGY CO., LTD..
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Device Details
Registration Details
f611dcc9351258d9dc80138938897bef
Ministry of Health Medical Device Manufacturing No. 009060
Product Details
Limited to the first level identification range of quality control materials (analytical and non-analytical) (A.1660) of the Measures for the Administration of Medical Devices.
A Clinical chemistry and clinical toxicology
A1660 Quality Control Materials (Analytical and Non-Analytical)
Produced in Taiwan, China
Dates and Status
Apr 27, 2021
Apr 27, 2026

