Taiwan FDA registration eaea8d51de9c87eb7436e1c611e9271b
Ushi Xinda automatic needle withdrawal pen
TW: 暐世信達自動退針採血筆
Taiwan·Risk Class 1·SUZHOU SPR MEDICAL DEVICES DEVELOPMENT CO., LTD.·Registered Aug 31, 2007 – Aug 31, 2012CancelledRegistration details
- Analysis ID
- eaea8d51de9c87eb7436e1c611e9271b
- Customs Code
- DHA04600042107
Company information
- Manufacturer
- SUZHOU SPR MEDICAL DEVICES DEVELOPMENT CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- VISGENEER, INC.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Aug 31, 2007
- Expiry Date
- Aug 31, 2012
- Cancellation Date
- Apr 14, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Ushi Xinda automatic needle withdrawal pen in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number eaea8d51de9c87eb7436e1c611e9271b and manufactured by SUZHOU SPR MEDICAL DEVICES DEVELOPMENT CO., LTD.. The authorized representative in Taiwan is VISGENEER, INC..
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