“Aesculap” General purpose medical instruments cleaner (Non-sterile) - Taiwan Registration a65e3f4412f7af633da743c74ea3f7af
Access comprehensive regulatory information for “Aesculap” General purpose medical instruments cleaner (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 a65e3f4412f7af633da743c74ea3f7af and manufactured by AESCULAP AG. The authorized representative in Taiwan is B. BRAUN TAIWAN 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
a65e3f4412f7af633da743c74ea3f7af
Ministry of Health Medical Device Import No. 021979
DHA09402197900
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
Sep 23, 2020
Sep 23, 2025

