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"Bard" Glide hemodialysis catheter - Taiwan Registration a5ea46a6aa21724182c477c336e0306b

Access comprehensive regulatory information for "Bard" Glide hemodialysis catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number a5ea46a6aa21724182c477c336e0306b 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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a5ea46a6aa21724182c477c336e0306b
Registration Details
Taiwan FDA Registration: a5ea46a6aa21724182c477c336e0306b
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Device Details

"Bard" Glide hemodialysis catheter
TW: "ๅทดๅพท" ่‘›่Šๅพท่ก€ๆถฒ้€ๆžๅฐŽ็ฎก
Risk Class 3
Cancelled

Registration Details

a5ea46a6aa21724182c477c336e0306b

DHA00601073704

Company Information

United States

Product Details

H Gastroenterology and urology

import

Dates and Status

Jul 01, 2004

Jul 01, 2019

May 19, 2022

Cancellation Information

Logged out

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