"Savyon" Helicobacter pylori Antigen Rapid Test (Non-Sterile) - Taiwan Registration 977ed0323dbec956d89a709ab7c3d205
Access comprehensive regulatory information for "Savyon" Helicobacter pylori Antigen Rapid Test (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 977ed0323dbec956d89a709ab7c3d205 and manufactured by SAVYON DIAGNOSTICS LTD.. The authorized representative in Taiwan is SEEKERS BIOMEDICAL 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
977ed0323dbec956d89a709ab7c3d205
Ministry of Health Medical Device Import No. 018776
DHA09401877602
Product Details
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Helicobacter Serological Reagent (C.0003)".
C Immunology and microbiology devices
C0003 Helicobacter serological reagent
Imported from abroad
Dates and Status
Jan 30, 2018
Jan 30, 2028

