Taiwan FDA registration 900ea6f5570adc9fff0683f5a331cc79

Baijie Youshan blood glucose test system

TW: 百捷優善血糖檢驗系統
Taiwan flagTaiwan·Risk Class 2·Qinli Biotechnology Co., Ltd. New North Plant·Registered Aug 04, 2022 – Aug 04, 2027Active
Registration details
Analysis ID
900ea6f5570adc9fff0683f5a331cc79
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
GENERAL LIFE BIOTECHNOLOGY CO., LTD.
Product details
Intended Use
This product can quantitatively detect the blood glucose concentration of fingertips, palms or forearm microvascular whole blood and venous blood. This system is suitable for home self-testing and professional detection of the patient's microvascular whole blood glucose concentration, and also suitable for professionals to detect the patient's venous blood glucose concentration.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1345 Glucose Test System
Import Information
QMS/QSD;; 國產
Dates and status
Registration Date
Aug 04, 2022
Expiry Date
Aug 04, 2027
About this record

Access comprehensive regulatory information for Baijie Youshan blood glucose test system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 900ea6f5570adc9fff0683f5a331cc79 and manufactured by Qinli Biotechnology Co., Ltd. New North Plant. The authorized representative in Taiwan is GENERAL LIFE BIOTECHNOLOGY CO., LTD..

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