Taiwan FDA registration be169ca671f8281e0ee330fb4b298e3f

“Hong Shiang” Ultrasonic diathermy

TW: “鴻祥”超音波治療儀

Taiwan·Risk Class 2·MD·HONG SHIANG TECHNOLOGY CO., LTD.·Registered Nov 08, 2016 – Nov 08, 2026Active

Registration details

Analysis ID: be169ca671f8281e0ee330fb4b298e3f
License Form: Ministry of Health Medical Device Manufacturing No. 005538

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): o Equipment for physical medicine
Product Type (Level 2): O5300 Ultrasonic Diathermy Therapy Device
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Nov 08, 2016
Expiry Date: Nov 08, 2026

About this record

Access comprehensive regulatory information for “Hong Shiang” Ultrasonic diathermy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number be169ca671f8281e0ee330fb4b298e3f and manufactured by HONG SHIANG TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is HONG SHIANG TECHNOLOGY CO., LTD..

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