Taiwan FDA registration ffe0f254a67ad06352a9f7162c27b089
“Storz” Masterpuls Shock Wave Therapy System and Accessories
TW: “思拓”邁氏波震波治療系統與配件
Taiwan·Risk Class 3·MD·Storz Medical AG·Registered Aug 26, 2016 – Aug 26, 2021ExpiredRegistration details
- Analysis ID
- ffe0f254a67ad06352a9f7162c27b089
- License Form
- Ministry of Health Medical Device Import No. 028750
- Customs Code
- DHA05602875009
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 Orthopedic devices
- Product Type (Level 2)
- N0001 Extracorporeal shock wave system for orthopedics
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 26, 2016
- Expiry Date
- Aug 26, 2021
About this record
Access comprehensive regulatory information for “Storz” 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 ffe0f254a67ad06352a9f7162c27b089 and manufactured by Storz Medical AG. The authorized representative in Taiwan is SHAWHAN BIOMEDICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices