High-concentration control serum for Fujifilm-dry chemical analyzers - Taiwan Registration f76673a38fd7a8b7a765d42ec499474f
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.
Device Details
Product Details
Slides for plasma and serum determination to confirm the accuracy and precision of the FUJI DRI-CHEM system.
A Clinical chemistry and clinical toxicology
A.1660 Quality control materials (analytical and non-analytical)
import
Dates and Status
Dec 13, 2005
Dec 13, 2025

