Pure Global

“Acandis” Derivo Embolisation Device - Taiwan Registration 497670d646f8b0d324d2db46bf291100

Access comprehensive regulatory information for “Acandis” Derivo Embolisation Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 497670d646f8b0d324d2db46bf291100 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
497670d646f8b0d324d2db46bf291100
Registration Details
Taiwan FDA Registration: 497670d646f8b0d324d2db46bf291100
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Acandis” Derivo Embolisation Device
TW: “艾康蒂”德瑞佛栓塞裝置
Risk Class 3
MD

Registration Details

497670d646f8b0d324d2db46bf291100

Ministry of Health Medical Device Import No. 031373

DHA05603137302

Company Information

Germany

Product Details

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

K Devices for neuroscience

K5950 Artificial embolization device

Imported from abroad

Dates and Status

Jul 27, 2018

Jul 27, 2028