Pure Global

“EucaTech” RESISTANT Self-Expandable Stent System - Taiwan Registration 5ac8e00976fcdbf8e1c8cafb39836398

Access comprehensive regulatory information for “EucaTech” RESISTANT Self-Expandable Stent System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5ac8e00976fcdbf8e1c8cafb39836398 and manufactured by eucatech AG. The authorized representative in Taiwan is SYNCESS 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
5ac8e00976fcdbf8e1c8cafb39836398
Registration Details
Taiwan FDA Registration: 5ac8e00976fcdbf8e1c8cafb39836398
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“EucaTech” RESISTANT Self-Expandable Stent System
TW: “優科德”里斯周邊血管支架系統
Risk Class 2
MD

Registration Details

5ac8e00976fcdbf8e1c8cafb39836398

Ministry of Health Medical Device Import No. 030788

DHA05603078800

Company Information

Germany

Product Details

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

E Cardiovascular devices

E0001 Cardiovascular stents

Imported from abroad

Dates and Status

Mar 28, 2018

Mar 28, 2028