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"Bard" Ike-Foss balloon expansion catheter - Taiwan Registration 03863bae680f8aa7e0b6c48ad233394b

Access comprehensive regulatory information for "Bard" Ike-Foss balloon expansion catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 03863bae680f8aa7e0b6c48ad233394b 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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03863bae680f8aa7e0b6c48ad233394b
Registration Details
Taiwan FDA Registration: 03863bae680f8aa7e0b6c48ad233394b
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Device Details

"Bard" Ike-Foss balloon expansion catheter
TW: โ€œๅทดๅพทโ€่‰พๅ…‹-ไฝ›ๆ–ฏๆฐฃ็ƒๆ“ดๅผตๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

03863bae680f8aa7e0b6c48ad233394b

DHA00601929606

Company Information

United States

Product Details

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

H Gastroenterology and urology

H.5470 ่ผธๅฐฟ็ฎกๆ“ดๅผตๅ™จ

import

Dates and Status

Oct 24, 2008

Oct 24, 2018

May 19, 2022

Cancellation Information

Logged out

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