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"Bossme" Custer peripheral vascular balloon dilation catheter - Taiwan Registration e1eb3f5e4b91e5dce05e73c1958a9c4b

Access comprehensive regulatory information for "Bossme" Custer 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 e1eb3f5e4b91e5dce05e73c1958a9c4b 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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e1eb3f5e4b91e5dce05e73c1958a9c4b
Registration Details
Taiwan FDA Registration: e1eb3f5e4b91e5dce05e73c1958a9c4b
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Device Details

"Bossme" Custer peripheral vascular balloon dilation catheter
TW: โ€œๅšไป•็พŽโ€ๅกๆ–ฏ็‰นๅ‘จ้‚Š่ก€็ฎกๆฐฃ็ƒๆ“ดๅผตๅฐŽ็ฎก
Risk Class 2

Registration Details

e1eb3f5e4b91e5dce05e73c1958a9c4b

DHA09200089908

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

Apr 16, 2018

Apr 16, 2028