Taiwan FDA registration 265e4a3e2a521361888e188dc81dc893
Fujifilm-Dry test piece for the determination of total bilirubin
TW: 富士-測定總膽紅素乾式試片
Taiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office·Registered Dec 13, 2005 – Dec 13, 2025ExpiredRegistration details
- Analysis ID
- 265e4a3e2a521361888e188dc81dc893
- Customs Code
- DHA00601554701
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- HUNG CHONG CORP.
Product details
- Intended Use
- Measures the concentration of total bilirubin in human plasma or serum.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1110 Bilirubin (total or direct) test system
- Import Information
- import
Dates and status
- Registration Date
- Dec 13, 2005
- Expiry Date
- Dec 13, 2025
About this record
Access comprehensive regulatory information for Fujifilm-Dry test piece for the determination of total bilirubin in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 265e4a3e2a521361888e188dc81dc893 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office. The authorized representative in Taiwan is HUNG CHONG CORP..
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