"Bard" Reflex balloon expansion catheter - Taiwan Registration a3558914bd7f34231fce636849cfc1b7
Access comprehensive regulatory information for "Bard" Reflex 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 a3558914bd7f34231fce636849cfc1b7 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.
Device Details
Product Details
For details, see Chinese Copycat Approved Version. Change efficiency: as detailed in Chinese copy of the copy.
E Cardiovascular Medicine Science
E.1250 Percutaneous catheters
import
Dates and Status
Jul 22, 2010
Jul 22, 2025

