Taiwan FDA registration 79eaf1ca23bd420f9a387ca718d2f1fc
Low concentration control serum for Fujifilm-Chem analyzer
TW: 富士-亁式化學分析儀用的低濃度對照血清
Taiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office·Registered Dec 19, 2005 – Dec 19, 2025ExpiredRegistration details
- Analysis ID
- 79eaf1ca23bd420f9a387ca718d2f1fc
- Customs Code
- DHA00601566201
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- HUNG CHONG CORP.
Product details
- Intended Use
- Plasma and serum assays were used to confirm the accuracy of the FUJI DRI-CHEM system using slides.
- 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
- import
Dates and status
- Registration Date
- Dec 19, 2005
- Expiry Date
- Dec 19, 2025
About this record
Access comprehensive regulatory information for Low concentration control serum for Fujifilm-Chem analyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 79eaf1ca23bd420f9a387ca718d2f1fc and manufactured by FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office. The authorized representative in Taiwan is HUNG CHONG CORP..
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