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"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.

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b748614c42a263358e6cf697687c5c6b
Registration Details
Taiwan FDA Registration: b748614c42a263358e6cf697687c5c6b
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Device Details

"Bossme" Emas peripheral vascular balloon dilation catheter
TW: โ€œๅšไป•็พŽโ€ ่‰พ็‘ชไป•ๅ‘จ้‚Š่ก€็ฎกๆฐฃ็ƒๆ“ดๅผตๅฐŽ็ฎก
Risk Class 2

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