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"Bard" Aitvans balloon expansion catheter - Taiwan Registration c55ec95523d005cc620cb695b8c75d5b

Access comprehensive regulatory information for "Bard" Aitvans 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 c55ec95523d005cc620cb695b8c75d5b and manufactured by BARD PERIPHERAL VASCULAR, 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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c55ec95523d005cc620cb695b8c75d5b
Registration Details
Taiwan FDA Registration: c55ec95523d005cc620cb695b8c75d5b
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Device Details

"Bard" Aitvans balloon expansion catheter
TW: โ€œๅทดๅพทโ€่‰พ็‰นๅ‡กๆ–ฏๆฐฃ็ƒๆ“ดๅผตๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

c55ec95523d005cc620cb695b8c75d5b

DHA00602022407

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Oct 05, 2009

Oct 05, 2014

May 28, 2018

Cancellation Information

Logged out

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