Pure Global

“Promedon” Vantris VUR Treatment System - Taiwan Registration d07d9f185158e891c08580a6aac7d697

Access comprehensive regulatory information for “Promedon” Vantris VUR Treatment System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number d07d9f185158e891c08580a6aac7d697 and manufactured by Promedon S.A.. The authorized representative in Taiwan is Foresee Medical 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
d07d9f185158e891c08580a6aac7d697
Registration Details
Taiwan FDA Registration: d07d9f185158e891c08580a6aac7d697
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Promedon” Vantris VUR Treatment System
TW: “博美敦”範逆勢膀胱輸尿管逆流治療系統
Risk Class 3
MD

Registration Details

d07d9f185158e891c08580a6aac7d697

Ministry of Health Medical Device Import No. 034254

DHA05603425409

Company Information

Argentina

Product Details

This product is used endoscopically to treat vesicoureteral reflux (VUR)

H Gastroenterology-urology devices

H9999 Other

Imported from abroad

Dates and Status

May 04, 2021

May 04, 2026