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"Bossme" Yaqili peripheral vascular balloon dilation catheter - Taiwan Registration 8eeed3d78e295ee244b47b9ddb2273f7

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).

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8eeed3d78e295ee244b47b9ddb2273f7
Registration Details
Taiwan FDA Registration: 8eeed3d78e295ee244b47b9ddb2273f7
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Device Details

"Bossme" Yaqili peripheral vascular balloon dilation catheter
TW: โ€œๅšไป•็พŽโ€ ้›…ๅ…ถๅˆฉๅ‘จ้‚Š่ก€็ฎกๆฐฃ็ƒๆ“ดๅผตๅฐŽ็ฎก
Risk Class 2

Registration Details

8eeed3d78e295ee244b47b9ddb2273f7

DHA09200089401

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

Contract manufacturing;; Input;; Chinese goods

Dates and Status

Mar 20, 2018

Mar 20, 2028