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"Bud" Aitvans 014/018 balloon expansion catheter - Taiwan Registration fb5885ea2f8d6eeff3512296a8391398

Access comprehensive regulatory information for "Bud" Aitvans 014/018 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 fb5885ea2f8d6eeff3512296a8391398 and manufactured by BARD PERIPHERAL VASCULAR, INC.;; CLEARSTREAM TECHNOLOGIES LTD.. 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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fb5885ea2f8d6eeff3512296a8391398
Registration Details
Taiwan FDA Registration: fb5885ea2f8d6eeff3512296a8391398
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Device Details

"Bud" Aitvans 014/018 balloon expansion catheter
TW: โ€œๅทดๅพทโ€่‰พ็‰นๅ‡กๆ–ฏ014/018ๆฐฃ็ƒๆ“ดๅผตๅฐŽ็ฎก
Risk Class 2

Registration Details

fb5885ea2f8d6eeff3512296a8391398

DHA00602495807

Company Information

Product Details

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

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

Contract manufacturing;; input

Dates and Status

May 28, 2013

May 28, 2028