Taiwan FDA registration d6abc766250ba73b5b4802a490822a96
"Pajani" ultrasound therapy device
TW: “帕佳尼”超音波治療儀
Taiwan·Risk Class 2·ELETTRONICA PAGANI SRL·Registered Mar 24, 2008 – Mar 24, 2018CancelledRegistration details
- Analysis ID
- d6abc766250ba73b5b4802a490822a96
- Customs Code
- DHA00601874007
Company information
- Manufacturer
- ELETTRONICA PAGANI SRL
- Manufacturer Country
- Italy
- Authorized Representative
- AMPLE MEDICAL INSTRUMENTS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- 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
- Mar 24, 2008
- Expiry Date
- Mar 24, 2018
- Cancellation Date
- Nov 26, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Pajani" ultrasound 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 d6abc766250ba73b5b4802a490822a96 and manufactured by ELETTRONICA PAGANI SRL. The authorized representative in Taiwan is AMPLE MEDICAL INSTRUMENTS CO., LTD..
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