Pure Global

“Acandis”NeuroBridge Catheter - Taiwan Registration 1f845e225568a786b5c7d9002eab00e0

Access comprehensive regulatory information for “Acandis”NeuroBridge Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1f845e225568a786b5c7d9002eab00e0 and manufactured by Acandis GmbH. The authorized representative in Taiwan is DR SHAO MD REGULATORY CONSULTANTS 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
1f845e225568a786b5c7d9002eab00e0
Registration Details
Taiwan FDA Registration: 1f845e225568a786b5c7d9002eab00e0
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Acandis”NeuroBridge Catheter
TW: “艾康蒂”諾布導管
Risk Class 2
MD

Registration Details

1f845e225568a786b5c7d9002eab00e0

Ministry of Health Medical Device Import No. 035412

DHA05603541206

Company Information

Germany

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E1250 Percutaneous catheter

Imported from abroad

Dates and Status

Apr 21, 2022

Apr 21, 2027