Taiwan FDA registration fa50ffd4f3791d9570d2a34360bcec5a
Reuterone body special product solution (unsterilized)
TW: 瑞特酮體專用品管液 (未滅菌)
Taiwan·Risk Class 1·Daqing Factory of Huaguang Biotechnology Co., Ltd·Registered Sep 06, 2022 – Sep 06, 2027ActiveRegistration details
- Analysis ID
- fa50ffd4f3791d9570d2a34360bcec5a
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Daqing Factory of Huaguang 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
- Sep 06, 2022
- Expiry Date
- Sep 06, 2027
About this record
Access comprehensive regulatory information for Reuterone body special product 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 fa50ffd4f3791d9570d2a34360bcec5a and manufactured by Daqing Factory of Huaguang Biotechnology Co., Ltd. The authorized representative in Taiwan is Daqing Factory of Huaguang Biotechnology Co., Ltd.
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