Taiwan FDA registration 225eb0d4124ca2d2fa4ad58ef85bffb1
"DORNIER" orthopedic extracorporeal shock wave therapy instrument
TW: “多尼爾”骨科體外震波治療儀
Taiwan·Risk Class 3·Dornier MedTech America, Inc.; DORNIER MEDTECH SYSTEMS GMBH·Registered May 21, 2007 – May 21, 2027ActiveRegistration details
- Analysis ID
- 225eb0d4124ca2d2fa4ad58ef85bffb1
- Customs Code
- DHA00601809007
Company information
- Manufacturer Country
- United States;;Germany
- Authorized Representative
- MEDEN INTERNATIONAL INC.
Product details
- Intended Use
- CALCIFIED TENDONITIS-肩鈣化性或非鈣化性肌腱炎,EPICONDYLITIS (TENNIS AND GOLF ELBOW)-肘上髁炎(網球肘),PLANTAR FASCIITIS (HEEL SPUR)-足底筋膜炎(腳踝骨刺),PSEUDARTHROSIS (NON-UNIONS)-骨折愈合不全(假性關節症).
- 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
- May 21, 2007
- Expiry Date
- May 21, 2027
About this record
Access comprehensive regulatory information for "DORNIER" orthopedic extracorporeal shock wave therapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 225eb0d4124ca2d2fa4ad58ef85bffb1 and manufactured by Dornier MedTech America, Inc.; DORNIER MEDTECH SYSTEMS GMBH. The authorized representative in Taiwan is MEDEN INTERNATIONAL INC..
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