Taiwan FDA registration 88d62df6e078e60cf372a050233ba7dd
"Pajani" physical shock wave therapy instrument
TW: “帕佳尼”物理震波治療儀
Taiwan·Risk Class 3·ELETTRONICA PAGANI SRL·Registered Mar 28, 2008 – Mar 28, 2018CancelledRegistration details
- Analysis ID
- 88d62df6e078e60cf372a050233ba7dd
- Customs Code
- DHA00601875507
Company information
- Manufacturer
- ELETTRONICA PAGANI SRL
- Manufacturer Country
- Italy
- Authorized Representative
- AMPLE MEDICAL INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Scapularized or non-calcified tendonitis, epicondylitis of the elbow (netball elbow), plantar fasciitis.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.0001 骨科用體外震波系統
- Import Information
- import
Dates and status
- Registration Date
- Mar 28, 2008
- Expiry Date
- Mar 28, 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" physical shock wave therapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 88d62df6e078e60cf372a050233ba7dd and manufactured by ELETTRONICA PAGANI SRL. The authorized representative in Taiwan is AMPLE MEDICAL INSTRUMENTS CO., LTD..
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