Taiwan FDA registration 25a6f5247e725aa1b2b0f5075f9bdbda
“Storz Medical” Masterpuls Shock Wave Therapy System and Accessories
TW: “斯拓茲”麥斯波震波治療系統
Taiwan·Risk Class 3·MD·Storz Medical AG·Registered May 28, 2018 – May 28, 2028ActiveRegistration details
- Analysis ID
- 25a6f5247e725aa1b2b0f5075f9bdbda
- License Form
- Ministry of Health Medical Device Import No. 031100
- Customs Code
- DHA05603110006
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)
- N Orthopedic devices
- Product Type (Level 2)
- N0001 Extracorporeal shock wave system for orthopedics
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 28, 2018
- Expiry Date
- May 28, 2028
About this record
Access comprehensive regulatory information for “Storz Medical” Masterpuls Shock Wave Therapy System and Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 25a6f5247e725aa1b2b0f5075f9bdbda and manufactured by Storz Medical AG. The authorized representative in Taiwan is KINDMED CORPORATION.
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