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"Bard" Reflex balloon expansion catheter - Taiwan Registration a3558914bd7f34231fce636849cfc1b7

Access comprehensive regulatory information for "Bard" Reflex balloon expansion catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a3558914bd7f34231fce636849cfc1b7 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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a3558914bd7f34231fce636849cfc1b7
Registration Details
Taiwan FDA Registration: a3558914bd7f34231fce636849cfc1b7
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Device Details

"Bard" Reflex balloon expansion catheter
TW: โ€œๅทดๅพทโ€้Šณๅญšๆฐฃ็ƒๆ“ดๅผตๅฐŽ็ฎก
Risk Class 2

Registration Details

a3558914bd7f34231fce636849cfc1b7

DHA00602126806

Company Information

United States

Product Details

For details, see Chinese Copycat Approved Version. Change efficiency: as detailed in Chinese copy of the copy.

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Jul 22, 2010

Jul 22, 2025