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“Bard” VascuTrak PTA Dilatation Catheter - Taiwan Registration 2919be88b483f2ba1c3f3c8eb18b3231

Access comprehensive regulatory information for “Bard” VascuTrak PTA Dilatation Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2919be88b483f2ba1c3f3c8eb18b3231 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.

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2919be88b483f2ba1c3f3c8eb18b3231
Registration Details
Taiwan FDA Registration: 2919be88b483f2ba1c3f3c8eb18b3231
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Device Details

“Bard” VascuTrak PTA Dilatation Catheter
TW: “巴德”維斯奇克經皮穿刺血管成形術導管
Risk Class 2
MD

Registration Details

2919be88b483f2ba1c3f3c8eb18b3231

Ministry of Health Medical Device Import No. 029426

DHA05602942605

Company Information

United States

Product Details

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

E Cardiovascular devices

E1250 Percutaneous catheter

Imported from abroad

Dates and Status

Mar 28, 2017

Mar 28, 2022