Pure Global

"BosMě" balloon dilation catheter - Taiwan Registration 0268dc62e9de00e666dc996d1de50f83

Access comprehensive regulatory information for "BosMě" balloon dilation catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0268dc62e9de00e666dc996d1de50f83 and manufactured by BrosMed Medical Co., Ltd.;; BrosMed Medical B.V.. The authorized representative in Taiwan is HAO YO ENTERPRISE CO., 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
0268dc62e9de00e666dc996d1de50f83
Registration Details
Taiwan FDA Registration: 0268dc62e9de00e666dc996d1de50f83
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"BosMě" balloon dilation catheter
TW: “博思邁”球囊擴張導管
Risk Class 2

Registration Details

0268dc62e9de00e666dc996d1de50f83

DHA09200124008

Company Information

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

Input;; Chinese goods

Dates and Status

Jul 21, 2021

Jul 21, 2026