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“Hexacath” Premounted Coronary Stent TITAN OPTIMAX - Taiwan Registration 705857b95b7ac2ffbae031bd4d2500b3

Access comprehensive regulatory information for “Hexacath” Premounted Coronary Stent TITAN OPTIMAX in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 705857b95b7ac2ffbae031bd4d2500b3 and manufactured by HEXACATH. The authorized representative in Taiwan is CATHERINE 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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705857b95b7ac2ffbae031bd4d2500b3
Registration Details
Taiwan FDA Registration: 705857b95b7ac2ffbae031bd4d2500b3
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Device Details

“Hexacath” Premounted Coronary Stent TITAN OPTIMAX
TW: “海斯凱”泰坦歐德邁冠狀動脈支架系統
Risk Class 3
MD

Registration Details

705857b95b7ac2ffbae031bd4d2500b3

Ministry of Health Medical Device Import No. 028148

DHA05602814801

Company Information

France

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

Jan 18, 2016

Jan 18, 2026