"Bossme" Emas peripheral vascular balloon dilation catheter - Taiwan Registration b748614c42a263358e6cf697687c5c6b
Access comprehensive regulatory information for "Bossme" Emas peripheral vascular balloon dilation catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b748614c42a263358e6cf697687c5c6b and manufactured by BrosMed Medical Co., Ltd.;; BrosMed Medical B.V.. The authorized representative in Taiwan is ANGEION MEDICAL INTERNATIONAL PTE. LTD. TAIWAN BRANCH (SINGAPORE).
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
Registration Details
b748614c42a263358e6cf697687c5c6b
DHA09200089309
Product Details
For details, it is Chinese approved copy of the imitation order
E Cardiovascular Medicine Science
E.1250 Percutaneous catheters
Chinese goods;; Contract manufacturing;; input
Dates and Status
Mar 20, 2018
Mar 20, 2028

