Pure Global

“Medtronic” CoreValve EnVeo PRO Delivery Catheter and Loading System - Taiwan Registration 9713653ca170af4c6204827980327158

Access comprehensive regulatory information for “Medtronic” CoreValve EnVeo PRO Delivery Catheter and Loading System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 9713653ca170af4c6204827980327158 and manufactured by MEDTRONIC IRELAND. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) 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
9713653ca170af4c6204827980327158
Registration Details
Taiwan FDA Registration: 9713653ca170af4c6204827980327158
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Medtronic” CoreValve EnVeo PRO Delivery Catheter and Loading System
TW: “美敦力”柯普經導管主動脈瓣膜輸送及裝載系統
Risk Class 3
MD

Registration Details

9713653ca170af4c6204827980327158

Ministry of Health Medical Device Import No. 034201

DHA05603420101

Company Information

Ireland

Product Details

Details such as Chinese change in the performance of the approved copy of the imitation order: details such as the approved Chinese manual (the original approved label, instruction manual or packaging on December 24, 109 will be withdrawn and invalidated).

E Cardiovascular devices

E3925 Heart valve replacement

Imported from abroad

Dates and Status

Dec 03, 2020

Dec 03, 2025