Taiwan FDA registration ebb625c76a0e3f09e11b43d7c800135b
"Baojian" extracorporeal shock wave therapy device
TW: "寶健" 體外震波治療儀
Taiwan·LITE-MED INC.·Registered Mar 20, 2006 – Mar 20, 2011CancelledRegistration details
- Analysis ID
- ebb625c76a0e3f09e11b43d7c800135b
Company information
- Manufacturer
- LITE-MED INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- LITE-MED INC.
Product details
- Intended Use
- 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
- Domestic
Dates and status
- Registration Date
- Mar 20, 2006
- Expiry Date
- Mar 20, 2011
- Cancellation Date
- Oct 29, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Baojian" extracorporeal shock wave therapy device in Taiwan's medical device market through Pure Global AI's free database. is registered under number ebb625c76a0e3f09e11b43d7c800135b and manufactured by LITE-MED INC.. The authorized representative in Taiwan is LITE-MED INC..
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