“Sebia” Hypergamma Control - Taiwan Registration 19bb1573572847aaae8b1b6d0001e81a
Access comprehensive regulatory information for “Sebia” Hypergamma Control in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 19bb1573572847aaae8b1b6d0001e81a and manufactured by SEBIA. The authorized representative in Taiwan is ARQon Medtech Co., Ltd..
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
Registration Details
19bb1573572847aaae8b1b6d0001e81a
Ministry of Health Medical Device Import No. 029320
DHA05602932002
Product Details
This product is used on HYDRAGEL, CAPILLARYS and MINICAP and other instruments as a quality control substance for human serum protein electrophoresis quantitative test.
A Clinical chemistry and clinical toxicology
A1660 Quality Control Materials (Analytical and Non-Analytical)
Imported from abroad
Dates and Status
Feb 07, 2017
Feb 07, 2027

