Fujifilm-assay creatine phosphate excitation/dry test piece - Taiwan Registration dad4eb6d0900aed98cc497362687ec58
Access comprehensive regulatory information for Fujifilm-assay creatine phosphate excitation/dry test piece in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dad4eb6d0900aed98cc497362687ec58 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
It is used to determine the concentration of CKMB in blood for plasma and serum use.
A Clinical chemistry and clinical toxicology
A.1215 Creatine phosphokinase/creatine kinase or isoenzyme testing system
import
Dates and Status
Jan 17, 2006
Jan 17, 2026