Kunxia immunoglobulin test set - Taiwan Registration 8b1097e3828330afb208bd5458a73054
Access comprehensive regulatory information for Kunxia immunoglobulin test set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8b1097e3828330afb208bd5458a73054 and manufactured by BIOKIT, S.A.. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).
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 product is used with the ARCHITECT c system to quantitatively test immunoglobulin E (IgE) in human serum or plasma.
A Clinical chemistry and clinical toxicology
A.1150 Calibrated Products
import
Dates and Status
Jan 30, 2012
Jan 30, 2027

