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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.

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181ee5e1d2ed37aa9af8735fd3e91de3
Registration Details
Taiwan FDA Registration: 181ee5e1d2ed37aa9af8735fd3e91de3
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Device Details

Uko needle moxibustion needle
TW: ๅฎ‡ๅ…‰้‡็ธ้‡
Risk Class 2
Cancelled

Registration Details

181ee5e1d2ed37aa9af8735fd3e91de3

DHA04200019301

Company Information

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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