"Bard" Glide hemodialysis catheter - Taiwan Registration a5ea46a6aa21724182c477c336e0306b
Access comprehensive regulatory information for "Bard" Glide hemodialysis catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number a5ea46a6aa21724182c477c336e0306b 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.
Free Database
Powered by Pure Global AI
89,000+ Devices
a5ea46a6aa21724182c477c336e0306b
Registration Details
Taiwan FDA Registration: a5ea46a6aa21724182c477c336e0306b
Device Details
"Bard" Glide hemodialysis catheter
TW: "ๅทดๅพท" ่่ๅพท่กๆถฒ้ๆๅฐ็ฎก
Risk Class 3
Cancelled

