Taiwan FDA registration fba0a32b75c17aef268d7b9d8e08c137
and light trace urine total protein standards
TW: 和光微量尿液總蛋白標準液
Taiwan·Risk Class 2·FUJIFILM WAKO PURE CHEMICAL CORPORATION MIE PLANT·Registered Apr 14, 2006 – Apr 14, 2026ExpiredRegistration details
- Analysis ID
- fba0a32b75c17aef268d7b9d8e08c137
- Customs Code
- DHA00601635000
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- MEDICARE PRODUCTS INC.
Product details
- Intended Use
- Together with Wako's reagents, it is used to determine the amount of protein or albumin in the urine.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1150 Calibrated Products
- Import Information
- import
Dates and status
- Registration Date
- Apr 14, 2006
- Expiry Date
- Apr 14, 2026
About this record
Access comprehensive regulatory information for and light trace urine total protein standards in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fba0a32b75c17aef268d7b9d8e08c137 and manufactured by FUJIFILM WAKO PURE CHEMICAL CORPORATION MIE PLANT. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..
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