Pure Global

“Baxter” Theranova - Taiwan Registration e296c5be0d1fd8738783d7618f7f7293

Access comprehensive regulatory information for “Baxter” Theranova in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e296c5be0d1fd8738783d7618f7f7293 and manufactured by GAMBRO DIALYSATOREN GMBH. The authorized representative in Taiwan is BAXTER HEALTHCARE 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
e296c5be0d1fd8738783d7618f7f7293
Registration Details
Taiwan FDA Registration: e296c5be0d1fd8738783d7618f7f7293
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Baxter” Theranova
TW: “百特”特腎力血液透析器
Risk Class 2
MD

Registration Details

e296c5be0d1fd8738783d7618f7f7293

Ministry of Health Medical Device Import No. 030686

DHA05603068605

Company Information

Germany

Product Details

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

H Gastroenterology-urology devices

H5860 Highly permeable hemodialysis system

Imported from abroad

Dates and Status

Jan 16, 2018

Jan 16, 2028