Taiwan FDA registration 232f073d013ef7ffc73da9aa0155e050
Fujifilm - Dry test piece for measuring direct bilirubin in blood
TW: 富士-測定血液中直接膽紅素乾式試片
Taiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office·Registered Feb 08, 2006 – Feb 08, 2026ExpiredRegistration details
- Analysis ID
- 232f073d013ef7ffc73da9aa0155e050
- Customs Code
- DHA00601597700
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- HUNG CHONG CORP.
Product details
- Intended Use
- Measure the concentration of direct bilirubin in 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
- Feb 08, 2006
- Expiry Date
- Feb 08, 2026
About this record
Access comprehensive regulatory information for Fujifilm - Dry test piece for measuring direct bilirubin 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 232f073d013ef7ffc73da9aa0155e050 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office. The authorized representative in Taiwan is HUNG CHONG CORP..
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