Taiwan FDA registration f20bfb94b135b21dae74b0099a146e8d
Fujifilm - Determination of albumin concentration test piece
TW: 富士-測定白蛋白濃度亁式試片
Taiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office·Registered Dec 13, 2005 – Dec 13, 2025ExpiredRegistration details
- Analysis ID
- f20bfb94b135b21dae74b0099a146e8d
- Customs Code
- DHA00601555408
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- HUNG CHONG CORP.
Product details
- Intended Use
- Measure albumin concentration in serum and plasma.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1035 Albumin Testing 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 - Determination of albumin concentration 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 f20bfb94b135b21dae74b0099a146e8d and manufactured by FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office. The authorized representative in Taiwan is HUNG CHONG CORP..
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