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“Bard “ PowerPort ClearVUE Slim Implantable Port - Taiwan Registration 34c212f9c51c199e274fb82c2f78521b

Access comprehensive regulatory information for “Bard “ PowerPort ClearVUE Slim 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 34c212f9c51c199e274fb82c2f78521b 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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34c212f9c51c199e274fb82c2f78521b
Registration Details
Taiwan FDA Registration: 34c212f9c51c199e274fb82c2f78521b
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Device Details

“Bard “ PowerPort ClearVUE Slim Implantable Port
TW: “巴德”威力克力育斯寧植入式注射座
Risk Class 2
MD

Registration Details

34c212f9c51c199e274fb82c2f78521b

Ministry of Health Medical Device Import No. 033931

DHA05603393107

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

Sep 02, 2020

Sep 02, 2025