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"Bud" Iquis' long-term hemodialysis catheter - Taiwan Registration 67830c9827a69d9934c5f0e9d54f9a8d

Access comprehensive regulatory information for "Bud" Iquis' long-term 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 67830c9827a69d9934c5f0e9d54f9a8d 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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67830c9827a69d9934c5f0e9d54f9a8d
Registration Details
Taiwan FDA Registration: 67830c9827a69d9934c5f0e9d54f9a8d
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Device Details

"Bud" Iquis' long-term hemodialysis catheter
TW: โ€œๅทดๅพทโ€ไผŠๅฅŽๆ–ฏ้•ทๆœŸๆ€ง่ก€ๆถฒ้€ๆžๅฐŽ็ฎก
Risk Class 3

Registration Details

67830c9827a69d9934c5f0e9d54f9a8d

DHA05602539003

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

Aug 30, 2013

Aug 30, 2028