Pure Global

“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.

Free Database
Powered by Pure Global AI
89,000+ Devices
a65e3f4412f7af633da743c74ea3f7af
Registration Details
Taiwan FDA Registration: a65e3f4412f7af633da743c74ea3f7af
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Aesculap” General purpose medical instruments cleaner (Non-sterile)
TW: “雅氏” 一般醫療器械用清潔劑(未滅菌)
Risk Class 1
MD

Registration Details

a65e3f4412f7af633da743c74ea3f7af

Ministry of Health Medical Device Import No. 021979

DHA09402197900

Company Information

Germany

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