Pure Global

“HONG SHIANG” MIDDLE FREQUENCY MULTIFUNCTION THERAPY UNIT - Taiwan Registration e3ac539f7d7e7e407bd0635da94fc4eb

Access comprehensive regulatory information for “HONG SHIANG” MIDDLE FREQUENCY MULTIFUNCTION THERAPY UNIT in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e3ac539f7d7e7e407bd0635da94fc4eb and manufactured by HONG SHIANG TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is HONG SHIANG 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
e3ac539f7d7e7e407bd0635da94fc4eb
Registration Details
Taiwan FDA Registration: e3ac539f7d7e7e407bd0635da94fc4eb
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“HONG SHIANG” MIDDLE FREQUENCY MULTIFUNCTION THERAPY UNIT
TW: “鴻祥”中頻多功能治療儀
Risk Class 2
MD

Registration Details

e3ac539f7d7e7e407bd0635da94fc4eb

Ministry of Health Medical Device Manufacturing No. 007095

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

K Devices for neuroscience

K5890 Transcutaneous electrical nerve stimulator for pain relief

Produced in Taiwan, China

Dates and Status

May 11, 2021

May 11, 2026