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“Bard” PowerPort ClearVUE isp Implantable Port - Taiwan Registration e5f9b98ef042e4d3d08e5f3e56a1e261

Access comprehensive regulatory information for “Bard” PowerPort ClearVUE isp Implantable Port in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e5f9b98ef042e4d3d08e5f3e56a1e261 and manufactured by BARD ACCESS SYSTEMS, 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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e5f9b98ef042e4d3d08e5f3e56a1e261
Registration Details
Taiwan FDA Registration: e5f9b98ef042e4d3d08e5f3e56a1e261
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Device Details

“Bard” PowerPort ClearVUE isp Implantable Port
TW: “巴德”威力克力育艾斯植入式注射座
Risk Class 2
MD

Registration Details

e5f9b98ef042e4d3d08e5f3e56a1e261

Ministry of Health Medical Device Import No. 033792

DHA05603379206

Company Information

United States

Product Details

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

J General hospital and personal use equipment

J5965 Subcutaneous implantable intravascular injection port and catheter

Imported from abroad

Dates and Status

Jul 15, 2020

Jul 15, 2025