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“CardioFocus” HeartLight Endoscopic Ablation System - Taiwan Registration dbe637011c94e9d2a31e22a3bd10259b

Access comprehensive regulatory information for “CardioFocus” HeartLight Endoscopic Ablation System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number dbe637011c94e9d2a31e22a3bd10259b and manufactured by CardioFocus, Inc.. The authorized representative in Taiwan is LORION ENTERPRISES INC..

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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dbe637011c94e9d2a31e22a3bd10259b
Registration Details
Taiwan FDA Registration: dbe637011c94e9d2a31e22a3bd10259b
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Device Details

“CardioFocus” HeartLight Endoscopic Ablation System
TW: “福客星”朗光內視鏡消融系統
Risk Class 3
MD

Registration Details

dbe637011c94e9d2a31e22a3bd10259b

Ministry of Health Medical Device Import No. 033810

DHA05603381008

Company Information

United States

Product Details

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

E Cardiovascular devices

E0008 Percutaneous puncture of cardiac ablation system

Imported from abroad

Dates and Status

Aug 07, 2020

Aug 07, 2025