Taiwan FDA registration 45477ff0cb0ebc25d9afc3d212e7bcb0
Hinda needle withdrawal lancet
TW: 欣達退針採血筆
Taiwan·Risk Class 1·WUXI XINDA MEDICAL DEVICE CO., LTD·Registered Mar 04, 2010 – Mar 04, 2015CancelledRegistration details
- Analysis ID
- 45477ff0cb0ebc25d9afc3d212e7bcb0
- Customs Code
- DHA04600088803
Company information
- Manufacturer
- WUXI XINDA MEDICAL DEVICE CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- HMD BIOMEDICAL 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
- Mar 04, 2010
- Expiry Date
- Mar 04, 2015
- Cancellation Date
- Jul 03, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Hinda needle withdrawal lancet in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 45477ff0cb0ebc25d9afc3d212e7bcb0 and manufactured by WUXI XINDA MEDICAL DEVICE CO., LTD. The authorized representative in Taiwan is HMD BIOMEDICAL INC..
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