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Twee to Triguide Balloon Dilatation Catheter - Taiwan Registration 51f441de1d855db484bc8b45f461fc01

Access comprehensive regulatory information for Twee to Triguide Balloon Dilatation Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 51f441de1d855db484bc8b45f461fc01 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, 1 companies making similar products including BrosMed Medical Co., Ltd.;; BrosMed Medical B.V., and 1 recent registrations in the same category. 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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51f441de1d855db484bc8b45f461fc01
Registration Details
Taiwan FDA Registration: 51f441de1d855db484bc8b45f461fc01
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Device Details

Twee to Triguide Balloon Dilatation Catheter
TW: ็‰นๅจ่‡ดไธ‰ๅฐŽ็ตฒ็ƒๅ›Šๆ“ดๅผตๅฐŽ็ฎก
Risk Class 2

Registration Details

51f441de1d855db484bc8b45f461fc01

DHA09200113600

Product Details

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

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

Input;; Chinese goods

Dates and Status

May 21, 2020

May 21, 2025

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