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"Bard" Speeda hemodialysis catheter - Taiwan Registration df7fe09c48fe9689c1f76b2bf19dfebf

Access comprehensive regulatory information for "Bard" Speeda hemodialysis catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number df7fe09c48fe9689c1f76b2bf19dfebf 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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df7fe09c48fe9689c1f76b2bf19dfebf
Registration Details
Taiwan FDA Registration: df7fe09c48fe9689c1f76b2bf19dfebf
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Device Details

"Bard" Speeda hemodialysis catheter
TW: โ€œๅทดๅพทโ€้€Ÿ้”่ก€ๆถฒ้€ๆžๅฐŽ็ฎก
Risk Class 2

Registration Details

df7fe09c48fe9689c1f76b2bf19dfebf

DHA00601777600

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

H Gastroenterology and urology

H.5540 Blood Access Devices and Accessories

import

Dates and Status

Mar 08, 2007

Mar 08, 2027