Taiwan FDA registration 7a9484be5cdcf493c1eef53aea114a1d
and photophosphocreatine stimulation/
TW: 和光磷肌酸激/
Taiwan·Risk Class 2·FUJIFILM WAKO PURE CHEMICAL CORPORATION MIE PLANT·Registered Jan 18, 2006 – Jan 18, 2026ExpiredRegistration details
- Analysis ID
- 7a9484be5cdcf493c1eef53aea114a1d
- Customs Code
- DHA00601590804
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- MEDICARE PRODUCTS INC.
Product details
- Intended Use
- Quantitatively detect creatine stirrup levels in serum or plasma.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1215 Creatine phosphokinase/creatine kinase or isoenzyme testing system
- Import Information
- import
Dates and status
- Registration Date
- Jan 18, 2006
- Expiry Date
- Jan 18, 2026
About this record
Access comprehensive regulatory information for and photophosphocreatine stimulation/ in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7a9484be5cdcf493c1eef53aea114a1d and manufactured by FUJIFILM WAKO PURE CHEMICAL CORPORATION MIE PLANT. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..
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