Taiwan FDA registration 09651c659a99cf7106913584d828c7fb
"Osti" extracorporeal shock wave lithotripter
TW: “奧斯堤”體外震波碎石機
Taiwan·Risk Class 2·AST GMBH·Registered Jan 26, 2010 – Jan 26, 2015CancelledRegistration details
- Analysis ID
- 09651c659a99cf7106913584d828c7fb
- Customs Code
- DHA00602056102
Company information
- Manufacturer
- AST GMBH
- Manufacturer Country
- Germany
- 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 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
- Jan 26, 2010
- Expiry Date
- Jan 26, 2015
- Cancellation Date
- Aug 14, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Osti" 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 09651c659a99cf7106913584d828c7fb and manufactured by AST GMBH. The authorized representative in Taiwan is LITHO MED TRADING CO., LTD..
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