"Helena" Capillary Serum Protein kit (Non-Sterile) - Taiwan Registration 2f8144172023dfb4b1671ade6b15a3bd
Access comprehensive regulatory information for "Helena" Capillary Serum Protein kit (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2f8144172023dfb4b1671ade6b15a3bd and manufactured by HELENA BIOSCIENCES EUROPE. The authorized representative in Taiwan is SHANG LI INSTRUMENTS 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
2f8144172023dfb4b1671ade6b15a3bd
Ministry of Health Medical Device Import No. 018970
DHA09401897001
Product Details
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Protein (Chemical Separation Method) Test System (A.1630)".
A Clinical chemistry and clinical toxicology
A1630 Protein (Chemical Separation) Test System
Imported from abroad
Dates and Status
Apr 16, 2018
Apr 16, 2023

