Taiwan FDA registration cde22ab3ac16682012aef5c97ed7bf42
“Storz” Duolith Shock Wave Therapy System and Accessories
TW: “思拓”多力震波治療系統與配件
Taiwan·Risk Class 3·MD·STORZ MEDICAL AG·Registered Dec 03, 2014 – Dec 03, 2019CancelledRegistration details
- Analysis ID
- cde22ab3ac16682012aef5c97ed7bf42
- License Form
- Ministry of Health Medical Device Import No. 026804
- Customs Code
- DHA05602680409
Company information
- Manufacturer
- STORZ MEDICAL AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- SHAWHAN BIOMEDICAL CO., LTD.
Product details
- 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
- Dec 03, 2014
- Expiry Date
- Dec 03, 2019
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “Storz” Duolith 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 cde22ab3ac16682012aef5c97ed7bf42 and manufactured by STORZ MEDICAL AG. The authorized representative in Taiwan is SHAWHAN BIOMEDICAL CO., LTD..
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