Taiwan FDA registration 6b5500c7ddd5044c1afc6a544f6259a7
“SONOLITH I-move” Extracorporeal Lithotripter
TW: “蘇諾里仕 艾莫孚”體外震波碎石機
Registration details
- Analysis ID
- 6b5500c7ddd5044c1afc6a544f6259a7
- License Form
- Department of Health Medical Device Import No. 022988
- Customs Code
- DHA00602298806
Company information
- Manufacturer
- EDAP TMS FRANCE
- Manufacturer Country
- France
- Authorized Representative
- LITHO MED TRADING CO., LTD.
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; The use of this equipment shall comply with the "Administrative Measures for the Implementation or Use of Specific Medical Technical Examination and Inspection Medical Equipment"
Dates and status
- Registration Date
- Nov 04, 2011
- Expiry Date
- Nov 04, 2026
About this record
Access comprehensive regulatory information for “SONOLITH I-move” Extracorporeal Lithotripter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6b5500c7ddd5044c1afc6a544f6259a7 and manufactured by EDAP TMS FRANCE. The authorized representative in Taiwan is LITHO MED TRADING CO., LTD..
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