Taiwan FDA registration 39692ecedea42ff9f9739daed7594e76
Medical technology low frequency therapy device
TW: 醫技低週波治療器
Taiwan·Risk Class 2·SHIAN JIA MEEI ENTERPRISE CO., LTD.·Registered Dec 05, 2018 – Dec 05, 2028ActiveRegistration details
- Analysis ID
- 39692ecedea42ff9f9739daed7594e76
Company information
- Manufacturer
- SHIAN JIA MEEI ENTERPRISE CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- E-GMED HEALTH CO., LTD
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.5890 Transcutaneous electrical nerve stimulator for pain relief
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Dec 05, 2018
- Expiry Date
- Dec 05, 2028
About this record
Access comprehensive regulatory information for Medical technology 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 39692ecedea42ff9f9739daed7594e76 and manufactured by SHIAN JIA MEEI ENTERPRISE CO., LTD.. The authorized representative in Taiwan is E-GMED HEALTH CO., LTD.
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