"GHope" Legionella (Non-Sterile) - Taiwan Registration 64f7c6d1c5d02e977a2acbdf540e0f1d
Access comprehensive regulatory information for "GHope" Legionella (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 64f7c6d1c5d02e977a2acbdf540e0f1d and manufactured by EIKEN CHEMICAL CO., LTD.. The authorized representative in Taiwan is GHOPE INTERNATIONAL BIOTECHNOLOGY 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
64f7c6d1c5d02e977a2acbdf540e0f1d
Ministry of Health Medical Device Import No. 019413
DHA09401941300
Product Details
C Immunology and microbiology devices
C3300 Haemophilus serology
Imported from abroad
Dates and Status
Jul 25, 2018
Jul 25, 2023
Jan 28, 2019
Cancellation Information
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