Taiwan FDA registration 85ad0c5fef048660285efd14fd2a3b38
Baijie ketone body quality control solution (unsterilized)
TW: 百捷酮體品管液 (未滅菌)
Taiwan·Risk Class 1·Qinli Biotechnology Co., Ltd. New North Plant·Registered Mar 31, 2022 – Mar 31, 2027ActiveRegistration details
- Analysis ID
- 85ad0c5fef048660285efd14fd2a3b38
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, quality control materials (analytical and non-analytical) (A.1660) the first level identification range.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1660 Quality control materials (analytical and non-analytical)
- Import Information
- QMS/QSD;; 國產
Dates and status
- Registration Date
- Mar 31, 2022
- Expiry Date
- Mar 31, 2027
About this record
Access comprehensive regulatory information for Baijie ketone body quality control solution (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 85ad0c5fef048660285efd14fd2a3b38 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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