Uko needle moxibustion needle - Taiwan Registration 181ee5e1d2ed37aa9af8735fd3e91de3
Access comprehensive regulatory information for Uko needle moxibustion needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 181ee5e1d2ed37aa9af8735fd3e91de3 and manufactured by SHANGHAI YANGLONG MEDICAL ARTICLES CO., LTD.. The authorized representative in Taiwan is YU Kuang Industrial 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.
J General hospital and personal use equipment
J.5580 Needle moxibustion needle
Input;; Chinese goods
Dates and Status
Mar 03, 2009
Mar 03, 2014
Dec 14, 2016
Cancellation Information
Logged out
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