Pure Global

“BenQ” Qflux Dialyzer - Taiwan Registration 481ba9e4ab795d905dddf0dc4c8cee7b

Access comprehensive regulatory information for “BenQ” Qflux Dialyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 481ba9e4ab795d905dddf0dc4c8cee7b and manufactured by BENQ DIALYSIS TECHNOLOGY CORP.. The authorized representative in Taiwan is BENQ DIALYSIS TECHNOLOGY CORP..

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
481ba9e4ab795d905dddf0dc4c8cee7b
Registration Details
Taiwan FDA Registration: 481ba9e4ab795d905dddf0dc4c8cee7b
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“BenQ” Qflux Dialyzer
TW: “明基”血液透析器
Risk Class 2
MD

Registration Details

481ba9e4ab795d905dddf0dc4c8cee7b

Ministry of Health Medical Device Manufacturing No. 006010

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order

H Gastroenterology-urology devices

H5860 Highly permeable hemodialysis system

Produced in Taiwan, China

Dates and Status

Dec 13, 2017

Dec 13, 2027