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"Weidekang" gastrointestinal biliary dilation balloon catheter - Taiwan Registration a0617e24350b46f589d4d0b2ebc3913b

Access comprehensive regulatory information for "Weidekang" gastrointestinal biliary dilation balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a0617e24350b46f589d4d0b2ebc3913b 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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a0617e24350b46f589d4d0b2ebc3913b
Registration Details
Taiwan FDA Registration: a0617e24350b46f589d4d0b2ebc3913b
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Device Details

"Weidekang" gastrointestinal biliary dilation balloon catheter
TW: โ€œๅ”ฏๅพทๅบทโ€่ƒƒ่…ธ่†ฝ้“ๆ“ดๅผตๆฐฃ็ƒๅฐŽ็ฎก
Risk Class 2

Registration Details

a0617e24350b46f589d4d0b2ebc3913b

DHA09200125903

Company Information

Product Details

Details are as detailed as approved Chinese instructions

H Gastroenterology and urology

H.5010 ่†ฝ็ฎก็”จๅฐŽ็ฎกๅŠๅ…ถ้™„ไปถ;; H.5365 ้ฃŸ้“ๆ“ดๅผตๅ™จ

Input;; Chinese goods

Dates and Status

Oct 25, 2021

Oct 25, 2026