Taiwan FDA registration 3dcd7cecc73e5fb9f6109d9d13f3b33c
Wuxi Xinda blood collection device
TW: 無錫信達採血器
Taiwan·Risk Class 1·WUXI XINDA MEDICAL DEVICE CO., LTD·Registered Mar 31, 2006 – Mar 31, 2011CancelledRegistration details
- Analysis ID
- 3dcd7cecc73e5fb9f6109d9d13f3b33c
- Customs Code
- DHA04600015502
Company information
- Manufacturer
- WUXI XINDA MEDICAL DEVICE CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- APEX BIOTECHNOLOGY CORPORATION
Product details
- Intended Use
- Limited to the first level identification range 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
- Mar 31, 2006
- Expiry Date
- Mar 31, 2011
- Cancellation Date
- Jan 21, 2013
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Wuxi Xinda blood collection device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3dcd7cecc73e5fb9f6109d9d13f3b33c and manufactured by WUXI XINDA MEDICAL DEVICE CO., LTD. The authorized representative in Taiwan is APEX BIOTECHNOLOGY CORPORATION.
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