Taiwan FDA registration 9dd5b0c88c52668e4b1ebd8dc90ff6e3
"Xinghui" Wangdi Double Action Weisting Liquid
TW: “杏輝”旺滴雙效濕潤液
Taiwan·Risk Class 2·SINPHAR PHARMACEUTICAL CO., LTD.·Registered Feb 08, 2010 – Dec 31, 2014CancelledRegistration details
- Analysis ID
- 9dd5b0c88c52668e4b1ebd8dc90ff6e3
- Customs Code
- DHY00500288506
Company information
- Manufacturer
- SINPHAR PHARMACEUTICAL CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SINPHAR PHARMACEUTICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.5928 Products for the preservation of soft contact lenses
- Import Information
- Domestic
Dates and status
- Registration Date
- Feb 08, 2010
- Expiry Date
- Dec 31, 2014
- Cancellation Date
- Nov 17, 2016
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Xinghui" Wangdi Double Action Weisting Liquid in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9dd5b0c88c52668e4b1ebd8dc90ff6e3 and manufactured by SINPHAR PHARMACEUTICAL CO., LTD.. The authorized representative in Taiwan is SINPHAR PHARMACEUTICAL CO., LTD..
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