Taiwan FDA registration 1281b55efa149a7f41c17a2c0960c8d0
"DORNIER" Ipos orthopedic shock wave therapy device
TW: "多尼爾" 伊波斯骨科震波治療儀
Taiwan·Risk Class 3·DORNIER MEDTECH SYSTEMS GMBH·Registered Sep 01, 2004 – Sep 01, 2024ExpiredRegistration details
- Analysis ID
- 1281b55efa149a7f41c17a2c0960c8d0
- Customs Code
- DHA00601082603
Company information
- Manufacturer
- DORNIER MEDTECH SYSTEMS GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- MEDEN INTERNATIONAL INC.
Product details
- Intended Use
- 足底筋膜炎(PLANTAR FASCIITIS).
- Product Type (Level 1)
- N Orthopedics
- Import Information
- import
Dates and status
- Registration Date
- Sep 01, 2004
- Expiry Date
- Sep 01, 2024
About this record
Access comprehensive regulatory information for "DORNIER" Ipos orthopedic 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 1281b55efa149a7f41c17a2c0960c8d0 and manufactured by DORNIER MEDTECH SYSTEMS GMBH. The authorized representative in Taiwan is MEDEN INTERNATIONAL INC..
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