Taiwan FDA registration 8b3526fd02e8b5b0920bc4bf01001179
“Sheng Yuan” Interferential Frequency Therapy Equipment
TW: “聖原”中頻向量治療儀
Taiwan·Risk Class 2·MD·Shengyuan Instrument Co., Ltd. Taoyuan Factory·Registered Jul 12, 2018 – Jul 12, 2028ActiveRegistration details
- Analysis ID
- 8b3526fd02e8b5b0920bc4bf01001179
- License Form
- Ministry of Health Medical Device Manufacturing No. 006132
Company information
- Manufacturer
- Shengyuan Instrument Co., Ltd. Taoyuan Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Shengyuan Instrument Co., Ltd. Taoyuan Factory
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)
- O5850 powered muscle stimulator
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jul 12, 2018
- Expiry Date
- Jul 12, 2028
About this record
Access comprehensive regulatory information for “Sheng Yuan” Interferential Frequency Therapy Equipment in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8b3526fd02e8b5b0920bc4bf01001179 and manufactured by Shengyuan Instrument Co., Ltd. Taoyuan Factory. The authorized representative in Taiwan is Shengyuan Instrument Co., Ltd. Taoyuan Factory.
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