Taiwan FDA registration d394a59d96aa94eb42891e8dc2ce7adf
BeneCheck β-Ketone Test Strip (Non-Sterile)
TW: 百捷 酮體試片 (未滅菌)
Registration details
- Analysis ID
- d394a59d96aa94eb42891e8dc2ce7adf
- License Form
- Ministry of Health Medical Device Manufacturing No. 008611
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 the "Ketone (Non-quantitative) Test System (A.1435)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1435 Ketone (non-quantitative) test system
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Sep 23, 2020
- Expiry Date
- Sep 23, 2025
About this record
Access comprehensive regulatory information for BeneCheck β-Ketone Test Strip (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 d394a59d96aa94eb42891e8dc2ce7adf 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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