“Bard” PowerGlide Pro Midline Catheter - Taiwan Registration 9138993237ca05500e2ca93dbdd7e044

Access comprehensive regulatory information for “Bard” PowerGlide Pro Midline Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9138993237ca05500e2ca93dbdd7e044 and manufactured by BARD ACCESS SYSTEMS, 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.