Taiwan FDA registration a341bb77e51a5e6dbb1b5d8bf685f09e
Fujifilm-Determination of blood creatine phosphokinase dry test piece
TW: 富士-測定血液肌酸磷酸激酶乾式試片
Taiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office·Registered Jan 05, 2006 – Jan 05, 2026ExpiredRegistration details
- Analysis ID
- a341bb77e51a5e6dbb1b5d8bf685f09e
- Customs Code
- DHA00601583605
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- HUNG CHONG CORP.
Product details
- Intended Use
- Measure the concentration of creatine phosphokinase in plasma or serum.
- 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 05, 2006
- Expiry Date
- Jan 05, 2026
About this record
Access comprehensive regulatory information for Fujifilm-Determination of blood creatine phosphokinase dry test piece in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a341bb77e51a5e6dbb1b5d8bf685f09e and manufactured by FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office. The authorized representative in Taiwan is HUNG CHONG CORP..
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