Taiwan FDA registration f611dcc9351258d9dc80138938897bef
BeneCheck β-Ketone Control Solution (Non-Sterile)
TW: 百捷 酮體品管液 (未滅菌)
Taiwan·Risk Class 1·MD·Qinli Biotechnology Co., Ltd. new tree factory·Registered Apr 27, 2021 – Apr 27, 2026ExpiredRegistration details
- Analysis ID
- f611dcc9351258d9dc80138938897bef
- License Form
- Ministry of Health Medical Device Manufacturing No. 009060
Company information
- Manufacturer
- Qinli Biotechnology Co., Ltd. new tree factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- GENERAL LIFE BIOTECHNOLOGY CO., LTD.
Product details
- Intended Use
- 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.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1660 Quality Control Materials (Analytical and Non-Analytical)
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Apr 27, 2021
- Expiry Date
- Apr 27, 2026
About this record
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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