Taiwan FDA registration 8e356817f6da8145f237abff991251dd
Fuji - Dry test piece for measuring creatinine concentration in blood
TW: 富士-測定血中肌酸酐濃度乾式試片
Taiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office·Registered Dec 14, 2005 – Dec 14, 2025ExpiredRegistration details
- Analysis ID
- 8e356817f6da8145f237abff991251dd
- Customs Code
- DHA00601556309
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- HUNG CHONG CORP.
Product details
- Intended Use
- Creatinine concentration is measured in plasma or serum.
- 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
- Dec 14, 2005
- Expiry Date
- Dec 14, 2025
About this record
Access comprehensive regulatory information for Fuji - Dry test piece for measuring creatinine concentration in blood in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8e356817f6da8145f237abff991251dd and manufactured by FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office. The authorized representative in Taiwan is HUNG CHONG CORP..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices