Taiwan FDA registration 581cf35484acea69880648dfc61688e2

Hong Shiang Transcutaneous Electrical Nerve Stimulator

TW: 鴻祥低週波治療器

Taiwan·Risk Class 2·MD·HONG SHIANG TECHNOLOGY CO., LTD.·Registered May 11, 2018 – May 11, 2028Active

Registration details

Analysis ID: 581cf35484acea69880648dfc61688e2
License Form: Ministry of Health Medical Device Manufacturing No. 006048

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: For details, it is Chinese approved copy of the imitation order
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, 2018
Expiry Date: May 11, 2028

About this record

Access comprehensive regulatory information for Hong Shiang Transcutaneous Electrical Nerve Stimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 581cf35484acea69880648dfc61688e2 and manufactured by HONG SHIANG TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is HONG SHIANG TECHNOLOGY CO., LTD..

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