Taiwan FDA registration 6193103dd8d267d36c701dd7e19bf8d1
and photocreatinine test system
TW: 和光肌酸酐試驗系統
Taiwan·Risk Class 2·FUJIFILM WAKO PURE CHEMICAL CORPORATION MIE PLANT·Registered Jan 18, 2006 – Jan 18, 2021CancelledRegistration details
- Analysis ID
- 6193103dd8d267d36c701dd7e19bf8d1
- Customs Code
- DHA00601591004
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- MEDICARE PRODUCTS INC.
Product details
- Intended Use
- Quantitatively detect creatinine content in serum or urine.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1225 肌氨酸酐試驗系統(Creatininetestsystem)
- Import Information
- import
Dates and status
- Registration Date
- Jan 18, 2006
- Expiry Date
- Jan 18, 2021
- Cancellation Date
- Oct 06, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for and photocreatinine test system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6193103dd8d267d36c701dd7e19bf8d1 and manufactured by FUJIFILM WAKO PURE CHEMICAL CORPORATION MIE PLANT. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..
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