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"Bard" Negiri dialysis catheter - Taiwan Registration 5c80b57f4cd09a9b9b0d5e1f5f689178

Access comprehensive regulatory information for "Bard" Negiri dialysis catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5c80b57f4cd09a9b9b0d5e1f5f689178 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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5c80b57f4cd09a9b9b0d5e1f5f689178
Registration Details
Taiwan FDA Registration: 5c80b57f4cd09a9b9b0d5e1f5f689178
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Device Details

"Bard" Negiri dialysis catheter
TW: "ๅทดๅพท" ่€ๅ‰็‘ž้€ๆžๅฐŽ็ฎก
Risk Class 2

Registration Details

5c80b57f4cd09a9b9b0d5e1f5f689178

DHA00601019000

Company Information

United States

Product Details

H Gastroenterology and urology

import

Dates and Status

Jan 22, 2003

Jan 22, 2028