Taiwan FDA registration dd3a1b37cc4909531601cb6160d6d8f3
Wako starch/
TW: 和光澱粉/
Taiwan·Risk Class 2·FUJIFILM WAKO PURE CHEMICAL CORPORATION MIE PLANT·Registered Jan 17, 2006 – Jan 17, 2026ExpiredRegistration details
- Analysis ID
- dd3a1b37cc4909531601cb6160d6d8f3
- Customs Code
- DHA00601589600
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- MEDICARE PRODUCTS INC.
Product details
- Intended Use
- The performance change (correction) is to quantitatively detect amylase activity in serum, plasma, and urine.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1070 澱粉酶試驗系統
- Import Information
- import
Dates and status
- Registration Date
- Jan 17, 2006
- Expiry Date
- Jan 17, 2026
About this record
Access comprehensive regulatory information for Wako starch/ in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dd3a1b37cc4909531601cb6160d6d8f3 and manufactured by FUJIFILM WAKO PURE CHEMICAL CORPORATION MIE PLANT. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..
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