and light B composite standard - Taiwan Registration 6c6eeb0f57b5e1f2f74fc524cb28f80c
Access comprehensive regulatory information for and light B composite standard in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6c6eeb0f57b5e1f2f74fc524cb28f80c and manufactured by FUJIFILM Wako Pure Chemical Corporation Mie Plant. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..
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
This standard solution with WAKO's reagents can be used to determine the content of glucose, uric acid, and urea nitrogen in human serum, plasma, or urine.
A Clinical chemistry and clinical toxicology
A.1150 Calibrated Products
import
Dates and Status
Dec 16, 2005
Dec 16, 2025