Taiwan FDA registration dd192f0f5192e62e29809e2059caff30
Jiao Bo low frequency therapy device
TW: 雃博低週波治療器
Taiwan·Risk Class 2·SUN-RAIN SYSTEM CORP.·Registered Aug 31, 2009 – Jul 10, 2012CancelledRegistration details
- Analysis ID
- dd192f0f5192e62e29809e2059caff30
- Customs Code
- DHY00500277502
Company information
- Manufacturer
- SUN-RAIN SYSTEM CORP.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SUN-RAIN SYSTEM CORP.
Product details
- Intended Use
- Relieves shoulder soreness and peripheral nerve paralysis.
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.5890 Transcutaneous electrical nerve stimulator for pain relief
- Import Information
- Domestic
Dates and status
- Registration Date
- Aug 31, 2009
- Expiry Date
- Jul 10, 2012
- Cancellation Date
- Apr 16, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Jiao Bo 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 dd192f0f5192e62e29809e2059caff30 and manufactured by SUN-RAIN SYSTEM CORP.. The authorized representative in Taiwan is SUN-RAIN SYSTEM CORP..
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