Taiwan FDA registration fee7cba08ec0d8eb577479d249326c76
"Senjamei" low frequency therapy device
TW: "仙佳美" 低週波治療器
Taiwan·Risk Class 2·SHIAN JIA MEEI ENTERPRISE CO., LTD.·Registered Jul 17, 2003 – Jul 17, 2028ActiveRegistration details
- Analysis ID
- fee7cba08ec0d8eb577479d249326c76
Company information
- Manufacturer
- SHIAN JIA MEEI ENTERPRISE CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SHIAN JIA MEEI ENTERPRISE CO., LTD.
Product details
- Product Type (Level 1)
- K Neuroscience
- Import Information
- Domestic
Dates and status
- Registration Date
- Jul 17, 2003
- Expiry Date
- Jul 17, 2028
About this record
Access comprehensive regulatory information for "Senjamei" 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 fee7cba08ec0d8eb577479d249326c76 and manufactured by SHIAN JIA MEEI ENTERPRISE CO., LTD.. The authorized representative in Taiwan is SHIAN JIA MEEI ENTERPRISE CO., LTD..
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