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“Bard” True Flow Valvuloplasty Perfusion Catheter - Taiwan Registration 1c64aebfbf8b8960f7879862d6bb9c1a

Access comprehensive regulatory information for “Bard” True Flow Valvuloplasty Perfusion Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1c64aebfbf8b8960f7879862d6bb9c1a 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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1c64aebfbf8b8960f7879862d6bb9c1a
Registration Details
Taiwan FDA Registration: 1c64aebfbf8b8960f7879862d6bb9c1a
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Device Details

“Bard” True Flow Valvuloplasty Perfusion Catheter
TW: “巴德”楚芙瓣膜成形術灌注導管
Risk Class 2
MD

Registration Details

1c64aebfbf8b8960f7879862d6bb9c1a

Ministry of Health Medical Device Import No. 030817

DHA05603081707

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

Apr 23, 2018

Apr 23, 2028