Taiwan FDA registration a8144130590f9d6f23ab3494781f82c7
"Zhaoen" orthopedic extracorporeal shock wave therapy instrument
TW: “兆恩”骨科體外震波治療儀
Taiwan·Risk Class 3·JOEUN MEDICAL CO., LTD·Registered May 05, 2009 – May 05, 2019CancelledRegistration details
- Analysis ID
- a8144130590f9d6f23ab3494781f82c7
- Customs Code
- DHA00601982902
Company information
- Manufacturer
- JOEUN MEDICAL CO., LTD
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- MEDEX BIOTECH INSTRUMENTS INC.
Product details
- Intended Use
- Plantar fasciitis (ankle spurs), supraelbow ankleitis (elbow elitis), scapular calfifying tendonitis.
- 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
- May 05, 2009
- Expiry Date
- May 05, 2019
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Zhaoen" orthopedic extracorporeal 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 a8144130590f9d6f23ab3494781f82c7 and manufactured by JOEUN MEDICAL CO., LTD. The authorized representative in Taiwan is MEDEX BIOTECH INSTRUMENTS INC..
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