Taiwan FDA registration 143e08974a76f4f1d37c2b8afe4a85f1
Fujifilm Blood Ammonia Analyzer (Unsterilized)
TW: "富士" 血氨分析儀 (未滅菌)
Taiwan·Risk Class 1·FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office·Registered Mar 11, 2015 – Mar 11, 2030ActiveRegistration details
- Analysis ID
- 143e08974a76f4f1d37c2b8afe4a85f1
- Customs Code
- DHA09401499405
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- HUNG CHONG CORP.
Product details
- Intended Use
- It is limited to the first-level identification scope of the "Blood Ammonia Test System (A.1065)" of the Measures for the Classification and Grading of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1065 血氨試驗系統
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Mar 11, 2015
- Expiry Date
- Mar 11, 2030
About this record
Access comprehensive regulatory information for Fujifilm Blood Ammonia Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 143e08974a76f4f1d37c2b8afe4a85f1 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office. The authorized representative in Taiwan is HUNG CHONG CORP..
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