Taiwan FDA registration 48d0fec6ebd9748eaf7f4f4a67dc747b
"Sturz" extracorporeal shock wave therapy instrument
TW: “斯特茲”體外震波治療儀
Taiwan·Risk Class 2·STORZ MEDICAL AG·Registered Aug 23, 2013 – Aug 23, 2028ActiveRegistration details
- Analysis ID
- 48d0fec6ebd9748eaf7f4f4a67dc747b
- Customs Code
- DHA05602538602
Company information
- Manufacturer
- STORZ MEDICAL AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- KINDMED CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5990 體外震波碎石器
- Import Information
- import
Dates and status
- Registration Date
- Aug 23, 2013
- Expiry Date
- Aug 23, 2028
About this record
Access comprehensive regulatory information for "Sturz" extracorporeal shock wave therapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 48d0fec6ebd9748eaf7f4f4a67dc747b and manufactured by STORZ MEDICAL AG. The authorized representative in Taiwan is KINDMED CORPORATION.
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