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"Bud" Ike-Foss nephrostomy balloon dilation catheter - Taiwan Registration 52c6ca855400bfa39e0273020fd8c076

Access comprehensive regulatory information for "Bud" Ike-Foss nephrostomy balloon dilation catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 52c6ca855400bfa39e0273020fd8c076 and manufactured by C.R. BARD, 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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52c6ca855400bfa39e0273020fd8c076
Registration Details
Taiwan FDA Registration: 52c6ca855400bfa39e0273020fd8c076
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Device Details

"Bud" Ike-Foss nephrostomy balloon dilation catheter
TW: โ€œๅทดๅพทโ€ ่‰พๅ…‹-ไฝ›ๆ–ฏ่…Ž้€ ๅฃๆ‰‹่ก“ๆฐฃ็ƒๆ“ดๅผตๅฐŽ็ฎก
Risk Class 2

Registration Details

52c6ca855400bfa39e0273020fd8c076

DHA00601925709

Company Information

United States

Product Details

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

H Gastroenterology and urology

import

Dates and Status

Oct 07, 2008

Oct 07, 2028