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“Acandis” Accero Stent - Taiwan Registration dabcefef8d072e223283f02521367215

Access comprehensive regulatory information for “Acandis” Accero Stent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number dabcefef8d072e223283f02521367215 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.

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dabcefef8d072e223283f02521367215
Registration Details
Taiwan FDA Registration: dabcefef8d072e223283f02521367215
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Device Details

“Acandis” Accero Stent
TW: “艾康蒂”艾榭兒支架
Risk Class 3
MD

Registration Details

dabcefef8d072e223283f02521367215

Ministry of Health Medical Device Import No. 032752

DHA05603275202

Company Information

Germany

Product Details

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

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K5950 Artificial embolization device

Imported from abroad

Dates and Status

Aug 03, 2019

Aug 03, 2024