“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.
Device Details
Registration Details
e3ac539f7d7e7e407bd0635da94fc4eb
Ministry of Health Medical Device Manufacturing No. 007095
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

