Taiwan FDA registration f52a4409742a7ffed220516a735a228c
"AGLA" uric acid test strip (unsterilized)
TW: "愛科來" 尿酸檢測試紙(未滅菌)
Taiwan·Risk Class 1·ARKRAY Factory, Inc.,Head office factory·Registered Dec 30, 2022 – Dec 30, 2027ActiveRegistration details
- Analysis ID
- f52a4409742a7ffed220516a735a228c
- Customs Code
- DHA09402299707
Company information
- Manufacturer
- ARKRAY Factory, Inc.,Head office factory
- Manufacturer Country
- Japan
- Authorized Representative
- SYNGEN BIOTECH 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;; 輸入
Dates and status
- Registration Date
- Dec 30, 2022
- Expiry Date
- Dec 30, 2027
About this record
Access comprehensive regulatory information for "AGLA" uric acid test strip (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f52a4409742a7ffed220516a735a228c and manufactured by ARKRAY Factory, Inc.,Head office factory. The authorized representative in Taiwan is SYNGEN BIOTECH CO., LTD..
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