Taiwan FDA registration e5d947833916743e20094db0c0376232
Fuji - Measuring whole blood glucose specimen
TW: 富士-測定全血血糖亁式試片
Taiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office·Registered Dec 19, 2005 – Dec 19, 2025ExpiredRegistration details
- Analysis ID
- e5d947833916743e20094db0c0376232
- Customs Code
- DHA00601567405
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- HUNG CHONG CORP.
Product details
- Intended Use
- Measure the blood glucose concentration in plasma or serum.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1345 Glucose Test System
- Import Information
- import
Dates and status
- Registration Date
- Dec 19, 2005
- Expiry Date
- Dec 19, 2025
About this record
Access comprehensive regulatory information for Fuji - Measuring whole blood glucose specimen in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e5d947833916743e20094db0c0376232 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office. The authorized representative in Taiwan is HUNG CHONG CORP..
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