Taiwan FDA registration e3ac539f7d7e7e407bd0635da94fc4eb

“HONG SHIANG” MIDDLE FREQUENCY MULTIFUNCTION THERAPY UNIT

TW: “鴻祥”中頻多功能治療儀

Taiwan·Risk Class 2·MD·HONG SHIANG TECHNOLOGY CO., LTD.·Registered May 11, 2021 – May 11, 2026Expired

Registration details

Analysis ID: e3ac539f7d7e7e407bd0635da94fc4eb
License Form: Ministry of Health Medical Device Manufacturing No. 007095

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: Details are as detailed as approved Chinese instructions
Product Type (Level 1): K Devices for neuroscience
Product Type (Level 2): K5890 Transcutaneous electrical nerve stimulator for pain relief
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: May 11, 2021
Expiry Date: May 11, 2026

About this record

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..

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