Taiwan FDA registration 9e689adb461fee69a1ab26501819896a
“Zimmer” GentlePro Shock Wave Therapy System
TW: “利麥爾”傑特普體外震波治療儀
Taiwan·Risk Class 3·MD·ZIMMER MEDIZINSYSTEME GMBH·Registered Jun 03, 2021 – Jun 03, 2026ExpiredRegistration details
- Analysis ID
- 9e689adb461fee69a1ab26501819896a
- License Form
- Ministry of Health Medical Device Import No. 034580
- Customs Code
- DHA05603458009
Company information
- Manufacturer
- ZIMMER MEDIZINSYSTEME GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- WOH MEDICAL CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- 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
- Jun 03, 2021
- Expiry Date
- Jun 03, 2026
About this record
Access comprehensive regulatory information for “Zimmer” GentlePro Shock Wave Therapy System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 9e689adb461fee69a1ab26501819896a and manufactured by ZIMMER MEDIZINSYSTEME GMBH. The authorized representative in Taiwan is WOH MEDICAL CO., LTD..
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