Pure Global

“Bard” FLAIR Endovascular Stent Graft - Taiwan Registration 6483afd87d90d8b3989ea5b297ec16d7

Access comprehensive regulatory information for “Bard” FLAIR Endovascular Stent Graft in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 6483afd87d90d8b3989ea5b297ec16d7 and manufactured by BARD PERIPHERAL VASCULAR, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE 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
6483afd87d90d8b3989ea5b297ec16d7
Registration Details
Taiwan FDA Registration: 6483afd87d90d8b3989ea5b297ec16d7
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Bard” FLAIR Endovascular Stent Graft
TW: “巴德”福萊爾周邊血管內套膜支架
Risk Class 3
MD

Registration Details

6483afd87d90d8b3989ea5b297ec16d7

Ministry of Health Medical Device Import No. 027268

DHA05602726803

Company Information

United States

Product Details

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

E Cardiovascular devices

Imported from abroad

Dates and Status

Apr 21, 2015

Apr 21, 2025