Taiwan FDA registration f47687f55f656fb58a445d7aeaab3e6e
"Jimio Oh" ultrasound diathermy therapy device
TW: "吉米歐"超音波透熱治療儀
Taiwan·Risk Class 2·GBO MEDIZINTECHNIK AG.·Registered Jan 08, 2007 – Jan 08, 2012CancelledRegistration details
- Analysis ID
- f47687f55f656fb58a445d7aeaab3e6e
- Customs Code
- DHA00601766705
Company information
- Manufacturer
- GBO MEDIZINTECHNIK AG.
- Manufacturer Country
- Germany
- Authorized Representative
- Yuanhong Instrument Co., Ltd
Product details
- Intended Use
- Relieves pain, muscle spasms and joint contraction.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.5300 超音波透熱治療儀
- Import Information
- import
Dates and status
- Registration Date
- Jan 08, 2007
- Expiry Date
- Jan 08, 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 "Jimio Oh" ultrasound diathermy 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 f47687f55f656fb58a445d7aeaab3e6e and manufactured by GBO MEDIZINTECHNIK AG.. The authorized representative in Taiwan is Yuanhong Instrument Co., Ltd.
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