Taiwan FDA registration 95969f249563e33f5f9675bf11afc0e2
"Hongxiang" low-frequency therapy device
TW: “鴻祥”低週波治療器
Taiwan·Risk Class 2·HONG SHIANG TECHNOLOGY CO., LTD.·Registered Sep 05, 2014 – Dec 24, 2024ExpiredRegistration details
- Analysis ID
- 95969f249563e33f5f9675bf11afc0e2
- Customs Code
- DHY00500285701
Company information
- Manufacturer
- HONG SHIANG TECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HONG SHIANG TECHNOLOGY CO., LTD.
Product details
- Intended Use
- Relieves shoulder soreness and peripheral nerve paralysis
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.5890 Transcutaneous electrical nerve stimulator for pain relief
- Import Information
- Domestic
Dates and status
- Registration Date
- Sep 05, 2014
- Expiry Date
- Dec 24, 2024
About this record
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..
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