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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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f611dcc9351258d9dc80138938897bef
Registration Details
Taiwan FDA Registration: f611dcc9351258d9dc80138938897bef
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Device Details

BeneCheck β-Ketone Control Solution (Non-Sterile)
TW: 百捷 酮體品管液 (未滅菌)
Risk Class 1
MD

Registration Details

f611dcc9351258d9dc80138938897bef

Ministry of Health Medical Device Manufacturing No. 009060

Company Information

Taiwan, Province of China

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