Taiwan FDA registration 9729a6f1211f0a16d4ffe213bed3b4ee
Uric Acid Tester Set (Unsterilized)
TW: 暐世尿酸測試儀套組(未滅菌)
Taiwan·Risk Class 1·Hsinchu General Factory of Weishi Biotechnology Co., Ltd·Registered Aug 09, 2022 – Aug 09, 2027ActiveRegistration details
- Analysis ID
- 9729a6f1211f0a16d4ffe213bed3b4ee
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Hsinchu General Factory of Weishi Biotechnology Co., Ltd
Product details
- Intended Use
- Limited to the first level identification scope of the "uric acid test system (A.1775)" of the Measures for the Classification and Grading Management of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1775 尿酸試驗系統
- Import Information
- QMS/QSD;; 國產
Dates and status
- Registration Date
- Aug 09, 2022
- Expiry Date
- Aug 09, 2027
About this record
Access comprehensive regulatory information for Uric Acid Tester Set (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9729a6f1211f0a16d4ffe213bed3b4ee and manufactured by Hsinchu General Factory of Weishi Biotechnology Co., Ltd. The authorized representative in Taiwan is Hsinchu General Factory of Weishi Biotechnology Co., Ltd.
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