Taiwan FDA registration 1e1381b0660536448b2518dc89f5d934
"Sunolis Amofu" extracorporeal shock wave lithotripsy
TW: “蘇諾里仕 艾莫孚”體外震波碎石機
Taiwan·Risk Class 2·EDAP TMS FRANCE·Registered Nov 04, 2011 – Nov 04, 2026ActiveRegistration details
- Analysis ID
- 1e1381b0660536448b2518dc89f5d934
- Customs Code
- DHA00602298806
Company information
- Manufacturer
- EDAP TMS FRANCE
- Manufacturer Country
- France
- Authorized Representative
- Lissot Trading Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5990 體外震波碎石器
- Import Information
- The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". input
Dates and status
- Registration Date
- Nov 04, 2011
- Expiry Date
- Nov 04, 2026
About this record
Access comprehensive regulatory information for "Sunolis Amofu" extracorporeal shock wave lithotripsy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1e1381b0660536448b2518dc89f5d934 and manufactured by EDAP TMS FRANCE. The authorized representative in Taiwan is Lissot Trading Co., Ltd.
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