Pure Global

“Genoss” PTCA Balloon Catheter - Taiwan Registration 6af4836b2f8789bb0a5a26014882e77e

Access comprehensive regulatory information for “Genoss” 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 6af4836b2f8789bb0a5a26014882e77e and manufactured by Genoss Co., Ltd.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.

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
6af4836b2f8789bb0a5a26014882e77e
Registration Details
Taiwan FDA Registration: 6af4836b2f8789bb0a5a26014882e77e
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Genoss” PTCA Balloon Catheter
TW: “吉諾司”冠狀動脈球囊導管
Risk Class 2
MD

Registration Details

6af4836b2f8789bb0a5a26014882e77e

Ministry of Health Medical Device Import No. 033226

DHA05603322602

Company Information

Korea, Republic of

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

Jan 22, 2020

Jan 22, 2025