Taiwan FDA registration 6c159fb987c7fd5ff855414413e470c9
BeneCheck ß-Ketone Test Strip (Non-Sterile)
TW: 百捷酮體試片 (未滅菌)
Taiwan·Risk Class 1·MD·Qinli Biotechnology Co., Ltd. New North Plant·Registered Mar 01, 2022 – Mar 01, 2027ActiveRegistration details
- Analysis ID
- 6c159fb987c7fd5ff855414413e470c9
- License Form
- Ministry of Health Medical Device Manufacturing No. 009478
Company information
- Manufacturer
- Qinli Biotechnology Co., Ltd. New North Plant
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- GENERAL LIFE BIOTECHNOLOGY CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment "Ketone (non-quantitative) test system (A.1435)" first level identification range.
- 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
- Mar 01, 2022
- Expiry Date
- Mar 01, 2027
About this record
Access comprehensive regulatory information for BeneCheck ß-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 6c159fb987c7fd5ff855414413e470c9 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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