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"Bard" intravenous indwelling catheter - Taiwan Registration 80c35614ca3ba5a9946d740c1da84d8d

Access comprehensive regulatory information for "Bard" intravenous indwelling catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 80c35614ca3ba5a9946d740c1da84d8d 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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80c35614ca3ba5a9946d740c1da84d8d
Registration Details
Taiwan FDA Registration: 80c35614ca3ba5a9946d740c1da84d8d
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Device Details

"Bard" intravenous indwelling catheter
TW: "ๅทดๅพท" ้œ่„ˆๆณจๅฐ„็•™็ฝฎๅฐŽ็ฎก
Risk Class 2

Registration Details

80c35614ca3ba5a9946d740c1da84d8d

DHA00600753304

Company Information

United States

Product Details

0399 Other artificial function substitutes

import

Dates and Status

Jul 07, 1995

Feb 09, 2029