Taiwan FDA registration 8eeed3d78e295ee244b47b9ddb2273f7

"Bossme" Yaqili peripheral vascular balloon dilation catheter

TW: “博仕美” 雅其利周邊血管氣球擴張導管
Taiwan flagTaiwan·Risk Class 2·BrosMed Medical Co., Ltd.;; BrosMed Medical B.V.·Registered Mar 20, 2018 – Mar 20, 2028Active
Registration details
Analysis ID
8eeed3d78e295ee244b47b9ddb2273f7
Customs Code
DHA09200089401
Company information
Manufacturer Country
Netherlands;;China
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
E Cardiovascular Medicine Science
Product Type (Level 2)
E.1250 Percutaneous catheters
Import Information
Contract manufacturing;; Input;; Chinese goods
Dates and status
Registration Date
Mar 20, 2018
Expiry Date
Mar 20, 2028
About this record

Access comprehensive regulatory information for "Bossme" Yaqili 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 8eeed3d78e295ee244b47b9ddb2273f7 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.

Free DatabasePowered by Pure Global AI89,000+ Devices