Fujifilm-Assay alkaline phosphatase dry test piece - Taiwan Registration 3556f32c1754fcccc19c7d83fe1a2dff
Access comprehensive regulatory information for Fujifilm-Assay alkaline phosphatase 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 3556f32c1754fcccc19c7d83fe1a2dff 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
Measure the concentration of Alkaline phosphatase in plasma or serum.
A Clinical chemistry and clinical toxicology
A.1050 Alkaline phosphatase or isoenzyme testing system
import
Dates and Status
Dec 14, 2005
Dec 14, 2025