Taiwan FDA registration 426f00840326b40bfbfd1ad9a55ba995
"Situo" Dooist orthopedic system with extracorporeal shock wave therapy
TW: “思拓”杜立斯骨科用體外震波治療系統
Taiwan·Risk Class 3·STORZ MEDICAL AG·Registered May 11, 2010 – May 11, 2015CancelledRegistration details
- Analysis ID
- 426f00840326b40bfbfd1ad9a55ba995
- Customs Code
- DHA00602100806
Company information
- Manufacturer
- STORZ MEDICAL AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- SHAWHAN BIOMEDICAL CO., LTD.
Product details
- Intended Use
- Condylitis of the elbow (tennis elbow), plantar fasciitis (condyle spurs of the foot).
- 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 11, 2010
- Expiry Date
- May 11, 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" Dooist orthopedic system with extracorporeal shock wave therapy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 426f00840326b40bfbfd1ad9a55ba995 and manufactured by STORZ MEDICAL AG. The authorized representative in Taiwan is SHAWHAN BIOMEDICAL CO., LTD..
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