Taiwan FDA registration 863ef4b5e5a907179957bd8026109062
Lux Blood Pen
TW: 樂適康採血筆
Taiwan·Risk Class 1·WUXI XINDA MEDICAL DEVICE CO., LTD·Registered Jun 20, 2007 – Jun 20, 2012CancelledRegistration details
- Analysis ID
- 863ef4b5e5a907179957bd8026109062
- Customs Code
- DHA04600039009
Company information
- Manufacturer
- WUXI XINDA MEDICAL DEVICE CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- U-E CHECK MEDICAL CO., LTD.
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
- Chinese goods;; input
Dates and status
- Registration Date
- Jun 20, 2007
- Expiry Date
- Jun 20, 2012
- Cancellation Date
- Jun 29, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Lux Blood Pen in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 863ef4b5e5a907179957bd8026109062 and manufactured by WUXI XINDA MEDICAL DEVICE CO., LTD. The authorized representative in Taiwan is U-E CHECK MEDICAL CO., LTD..
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