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"Weili" single-use minimally invasive dilation drainage kit - Taiwan Registration bf2f48247a58d2bab3b2c216c01a7188

Access comprehensive regulatory information for "Weili" single-use minimally invasive dilation drainage kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bf2f48247a58d2bab3b2c216c01a7188 and manufactured by WELL LEAD MEDICAL CO., LTD.. The authorized representative in Taiwan is Kang Cheng Medical Technology Co., Ltd.

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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bf2f48247a58d2bab3b2c216c01a7188
Registration Details
Taiwan FDA Registration: bf2f48247a58d2bab3b2c216c01a7188
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Device Details

"Weili" single-use minimally invasive dilation drainage kit
TW: โ€œ็ถญๅŠ›โ€ไธ€ๆฌกๆ€งไฝฟ็”จๅพฎๅ‰ตๆ“ดๅผตๅผ•ๆตๅฅ—ไปถ
Risk Class 2

Registration Details

bf2f48247a58d2bab3b2c216c01a7188

DHA09200094209

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

Jul 19, 2018

Jul 19, 2028