Taiwan FDA registration b748614c42a263358e6cf697687c5c6b

"Bossme" Emas peripheral vascular balloon dilation catheter

TW: “博仕美” 艾瑪仕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
b748614c42a263358e6cf697687c5c6b
Customs Code
DHA09200089309
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
Chinese goods;; Contract manufacturing;; input
Dates and status
Registration Date
Mar 20, 2018
Expiry Date
Mar 20, 2028
About this record

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).

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