Taiwan FDA registration b57b93a06e660aa9f461cda270e0d38a
and light amylase
TW: 和光澱粉酶
Taiwan·Risk Class 2·FUJIFILM Wako Pure Chemical Corporation Mie Plant·Registered Oct 03, 2023 – Oct 03, 2028ActiveRegistration details
- Analysis ID
- b57b93a06e660aa9f461cda270e0d38a
- Customs Code
- DHA05603622703
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- MEDICARE PRODUCTS INC.
Product details
- Intended Use
- This product is used 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
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Oct 03, 2023
- Expiry Date
- Oct 03, 2028
About this record
Access comprehensive regulatory information for and light amylase in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b57b93a06e660aa9f461cda270e0d38a and manufactured by FUJIFILM Wako Pure Chemical Corporation Mie Plant. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..
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