Taiwan FDA registration f4492dcc0051cc26e0e695cbed6cb6d8
and light urine microalbumin reagent (unsterilized)
TW: 和光 尿液微量白蛋白試劑 (未滅菌)
Taiwan·Risk Class 1·FUJIFILM WAKO PURE CHEMICAL CORPORATION MIE PLANT·Registered Jan 05, 2007 – Jan 05, 2027ActiveRegistration details
- Analysis ID
- f4492dcc0051cc26e0e695cbed6cb6d8
- Customs Code
- DHA04400550203
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- MEDICARE PRODUCTS INC.
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment "albumin immunoassay system (C.5040)" first level recognition range.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.5040 白蛋白免疫試驗系統
- Import Information
- import
Dates and status
- Registration Date
- Jan 05, 2007
- Expiry Date
- Jan 05, 2027
About this record
Access comprehensive regulatory information for and light urine microalbumin reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f4492dcc0051cc26e0e695cbed6cb6d8 and manufactured by FUJIFILM WAKO PURE CHEMICAL CORPORATION MIE PLANT. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..
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