Pure Global

“EucaTech” euca VI PTCA Balloon Catheter - Taiwan Registration 49d12f151d9b7529527a5277aa4dd557

Access comprehensive regulatory information for “EucaTech” euca VI PTCA Balloon Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 49d12f151d9b7529527a5277aa4dd557 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
49d12f151d9b7529527a5277aa4dd557
Registration Details
Taiwan FDA Registration: 49d12f151d9b7529527a5277aa4dd557
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“EucaTech” euca VI PTCA Balloon Catheter
TW: “優科德”優科第六代冠狀動脈氣球擴張導管
Risk Class 2
MD

Registration Details

49d12f151d9b7529527a5277aa4dd557

Ministry of Health Medical Device Import No. 030722

DHA05603072209

Company Information

Germany

Product Details

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

E Cardiovascular devices

E0005 Percutaneous puncture of the coronary ductus

Imported from abroad

Dates and Status

Feb 05, 2018

Feb 05, 2028