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"Weidekang" non-vascular luminal guide wire - Taiwan Registration f426172125026d35d3504fa07f17c4d7

Access comprehensive regulatory information for "Weidekang" non-vascular luminal guide wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f426172125026d35d3504fa07f17c4d7 and manufactured by JIANGSU VEDKANG MEDICAL SCIENCE & TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is CHINA SPRING TRADING CO., LTD..

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f426172125026d35d3504fa07f17c4d7
Registration Details
Taiwan FDA Registration: f426172125026d35d3504fa07f17c4d7
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Device Details

"Weidekang" non-vascular luminal guide wire
TW: โ€œๅ”ฏๅพทๅบทโ€้ž่ก€็ฎก่…”้“ๅฐŽๅผ•็ทš
Risk Class 2

Registration Details

f426172125026d35d3504fa07f17c4d7

DHA09200117500

Company Information

Product Details

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

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

Input;; Chinese goods

Dates and Status

Nov 17, 2020

Nov 17, 2025