Taiwan FDA registration 01cdcd77e1c32635757f7749d21347d0
“Dornier” Extracorporeal shock wave Lithotripter
TW: “多尼爾”體外震波碎石機
Taiwan·Risk Class 2·MD·DORNIER MEDTECH SYSTEMS GMBH·Registered Dec 13, 2016 – Dec 13, 2026ActiveRegistration details
- Analysis ID
- 01cdcd77e1c32635757f7749d21347d0
- License Form
- Ministry of Health Medical Device Import No. 029213
- Customs Code
- DHA05602921301
Company information
- Manufacturer
- DORNIER MEDTECH SYSTEMS GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- MEDEN INTERNATIONAL INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H5990 Extracorporeal shock wave lithotripsy
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 13, 2016
- Expiry Date
- Dec 13, 2026
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 01cdcd77e1c32635757f7749d21347d0 and manufactured by DORNIER MEDTECH SYSTEMS GMBH. The authorized representative in Taiwan is MEDEN INTERNATIONAL INC..
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