Taiwan FDA registration f6db316d54119061c9d59933b51cd6b4
"DORNIER" bone shock wave therapy device
TW: “多尼爾”骨震波治療儀
Taiwan·Risk Class 3·DORNIER MEDTECH SYSTEMS GMBH;;DORNIER MEDTECH GMBH·Registered Jun 24, 2016 – Jun 24, 2021CancelledRegistration details
- Analysis ID
- f6db316d54119061c9d59933b51cd6b4
- Customs Code
- DHA05602867202
Company information
- Manufacturer Country
- Germany
- Authorized Representative
- VICTORY EIGHT ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.0001 骨科用體外震波系統
- Import Information
- import
Dates and status
- Registration Date
- Jun 24, 2016
- Expiry Date
- Jun 24, 2021
- Cancellation Date
- Jun 15, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "DORNIER" bone shock wave therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number f6db316d54119061c9d59933b51cd6b4 and manufactured by DORNIER MEDTECH SYSTEMS GMBH;;DORNIER MEDTECH GMBH. The authorized representative in Taiwan is VICTORY EIGHT ENTERPRISE 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