Taiwan FDA registration bc5e6024e9a3c2566e83908145792906
"Fujifilm" Blood Ammonia Quality Control Solution (Unsterilized)
TW: "富士" 血氨品質控制液 (未滅菌)
Taiwan·Risk Class 1·FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office·Registered Sep 14, 2011 – Sep 14, 2026ActiveRegistration details
- Analysis ID
- bc5e6024e9a3c2566e83908145792906
- Customs Code
- DHA04401083103
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- HUNG CHONG CORP.
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment, quality control materials (analytical and non-analytical) (A.1660) the first level identification range.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1660 Quality control materials (analytical and non-analytical)
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Sep 14, 2011
- Expiry Date
- Sep 14, 2026
About this record
Access comprehensive regulatory information for "Fujifilm" Blood Ammonia Quality Control Solution (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bc5e6024e9a3c2566e83908145792906 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office. The authorized representative in Taiwan is HUNG CHONG CORP..
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