"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.
Device Details
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

