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"Hongxiang" low-frequency therapy device - Taiwan Registration 95969f249563e33f5f9675bf11afc0e2

Access comprehensive regulatory information for "Hongxiang" low-frequency therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 95969f249563e33f5f9675bf11afc0e2 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.

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95969f249563e33f5f9675bf11afc0e2
Registration Details
Taiwan FDA Registration: 95969f249563e33f5f9675bf11afc0e2
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Device Details

"Hongxiang" low-frequency therapy device
TW: โ€œ้ดป็ฅฅโ€ไฝŽ้€ฑๆณขๆฒป็™‚ๅ™จ
Risk Class 2

Registration Details

95969f249563e33f5f9675bf11afc0e2

DHY00500285701

Company Information

Taiwan, Province of China

Product Details

Relieves shoulder soreness and peripheral nerve paralysis

K Neuroscience

K.5890 Transcutaneous electrical nerve stimulator for pain relief

Domestic

Dates and Status

Sep 05, 2014

Dec 24, 2024