Taiwan FDA registration aeecdebca5fa5778858e733c4da9367f
"Situo" Misterpa orthopedic shock wave therapy system
TW: “思拓”米斯特帕骨科震波治療系統
Taiwan·Risk Class 3·STORZ MEDICAL AG·Registered Aug 02, 2010 – Aug 02, 2015CancelledRegistration details
- Analysis ID
- aeecdebca5fa5778858e733c4da9367f
- Customs Code
- DHA00602129203
Company information
- Manufacturer
- STORZ MEDICAL AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- SHAWHAN BIOMEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- 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
- Aug 02, 2010
- Expiry Date
- Aug 02, 2015
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Situo" Misterpa orthopedic shock wave therapy system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number aeecdebca5fa5778858e733c4da9367f and manufactured by STORZ MEDICAL AG. The authorized representative in Taiwan is SHAWHAN BIOMEDICAL CO., LTD..
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