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“EucaTech” euca CCFlex Coronary Stent System - Taiwan Registration 1390e3cb4acd67d579af82160213911e

Access comprehensive regulatory information for “EucaTech” euca CCFlex Coronary Stent System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 1390e3cb4acd67d579af82160213911e 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.

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1390e3cb4acd67d579af82160213911e
Registration Details
Taiwan FDA Registration: 1390e3cb4acd67d579af82160213911e
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Device Details

“EucaTech” euca CCFlex Coronary Stent System
TW: “優科德”優科喜福來冠狀動脈支架系統
Risk Class 3
MD

Registration Details

1390e3cb4acd67d579af82160213911e

Ministry of Health Medical Device Import No. 031520

DHA05603152002

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

Sep 10, 2018

Sep 10, 2028