Taiwan FDA registration e0ab371d3d904cb879acc324fb62e3f8
"Shujiang" uric acid reagent set (unsterilized)
TW: 〝朕江〞尿酸試劑套組(未滅菌)
Taiwan·Risk Class 1·LANNER BIOTECHNOLOGY CO., LTD.·Registered Jul 14, 2022 – Jul 14, 2027ActiveRegistration details
- Analysis ID
- e0ab371d3d904cb879acc324fb62e3f8
Company information
- Manufacturer
- LANNER BIOTECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- LANNER 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
- Jul 14, 2022
- Expiry Date
- Jul 14, 2027
About this record
Access comprehensive regulatory information for "Shujiang" uric acid reagent 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 e0ab371d3d904cb879acc324fb62e3f8 and manufactured by LANNER BIOTECHNOLOGY CO., LTD.. The authorized representative in Taiwan is LANNER BIOTECHNOLOGY CO., LTD..
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