“Muller-Omicron” Disinfectant (Non-Sterile) - Taiwan Registration 497a520ae13f86791c134f99e177b661
Access comprehensive regulatory information for “Muller-Omicron” Disinfectant (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 497a520ae13f86791c134f99e177b661 and manufactured by Muller-Omicron GmbH & Co. KG. The authorized representative in Taiwan is E.S.T. BIOTECH INC..
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
497a520ae13f86791c134f99e177b661
Ministry of Health Medical Device Import No. 020948
DHA09402094800
Product Details
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Disinfectants for General Medical Devices (J.6890)".
J General hospital and personal use equipment
J6890 Disinfectants for general medical devices
Imported from abroad
Dates and Status
Oct 15, 2019
Oct 15, 2024