Taiwan FDA registration 646c18f258b4ace2bca8716767ffddbe
"Wissharp" laparoscopic perfusion device
TW: "威夏普"腹腔鏡灌入器
Taiwan·Risk Class 2·WISAP GESELLCHAFT FÜR WISSENSCHAFTLICHEN APPARATEDAU MBH·Registered Jul 11, 2006 – Jul 11, 2016CancelledRegistration details
- Analysis ID
- 646c18f258b4ace2bca8716767ffddbe
- Customs Code
- DHA00601685909
Company information
- Manufacturer Country
- Germany
- Authorized Representative
- BEAMED INSTRUMENTS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- l Obstetrics and Gynecology
- Product Type (Level 2)
- L.1730 腹腔鏡灌入器
- Import Information
- import
Dates and status
- Registration Date
- Jul 11, 2006
- Expiry Date
- Jul 11, 2016
- Cancellation Date
- Oct 23, 2015
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Wissharp" laparoscopic perfusion device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 646c18f258b4ace2bca8716767ffddbe and manufactured by WISAP GESELLCHAFT FÜR WISSENSCHAFTLICHEN APPARATEDAU MBH. The authorized representative in Taiwan is BEAMED INSTRUMENTS CO., LTD..
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