Taiwan FDA registration f22ed1d6a07e3823731efbd457bf7875
"DORNIER" extracorporeal shock wave lithotripter
TW: "多尼爾 "體外震波碎石機
Taiwan·Risk Class 2·Dornier MedTech America, Inc.; DORNIER MEDTECH SYSTEMS GMBH·Registered Jul 26, 1994 – Feb 09, 2029ActiveRegistration details
- Analysis ID
- f22ed1d6a07e3823731efbd457bf7875
- Customs Code
- DHAS0600725905
Company information
- Manufacturer Country
- United States;;Germany
- Authorized Representative
- MEDEN INTERNATIONAL INC.
Product details
- Intended Use
- vacuum
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5990 體外震波碎石器
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Jul 26, 1994
- Expiry Date
- Feb 09, 2029
About this record
Access comprehensive regulatory information for "DORNIER" extracorporeal shock wave lithotripter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f22ed1d6a07e3823731efbd457bf7875 and manufactured by Dornier MedTech America, Inc.; DORNIER MEDTECH SYSTEMS GMBH. The authorized representative in Taiwan is MEDEN INTERNATIONAL INC..
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