Pure Global

“ASAHI” PTCA GUIDE WIRE - Taiwan Registration 78324bc01e91472737a7de83f0361740

Access comprehensive regulatory information for “ASAHI” PTCA GUIDE WIRE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 78324bc01e91472737a7de83f0361740 and manufactured by ASAHI INTECC(THAILAND) CO., LTD. The authorized representative in Taiwan is ASAHI INTECC CO.,LTD. TAIWAN BRANCH (JAPAN).

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
78324bc01e91472737a7de83f0361740
Registration Details
Taiwan FDA Registration: 78324bc01e91472737a7de83f0361740
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“ASAHI” PTCA GUIDE WIRE
TW: “朝日”冠狀動脈導引線
Risk Class 2
MD

Registration Details

78324bc01e91472737a7de83f0361740

Ministry of Health Medical Device Import No. 026204

DHA05602620401

Company Information

Product Details

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

E Cardiovascular devices

E1330 Catheter Lead

Imported from abroad

Dates and Status

May 20, 2014

May 20, 2024