Taiwan FDA registration f76673a38fd7a8b7a765d42ec499474f
High-concentration control serum for Fujifilm-dry chemical analyzers
TW: 富士-乾式化學分析儀用的高濃度對照血清
Taiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office·Registered Dec 13, 2005 – Dec 13, 2025ExpiredRegistration details
- Analysis ID
- f76673a38fd7a8b7a765d42ec499474f
- Customs Code
- DHA00601556207
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- HUNG CHONG CORP.
Product details
- Intended Use
- Slides for plasma and serum determination to confirm the accuracy and precision of the FUJI DRI-CHEM system.
- 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 13, 2005
- Expiry Date
- Dec 13, 2025
About this record
Access comprehensive regulatory information for High-concentration control serum for Fujifilm-dry chemical analyzers in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f76673a38fd7a8b7a765d42ec499474f and manufactured by FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office. The authorized representative in Taiwan is HUNG CHONG CORP..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices