Taiwan FDA registration 9f3e67183273c123d6d324c10c2e321b
Ruikang blood collection pen and blood lancet needle
TW: 瑞康採血筆及採血針
Taiwan·Risk Class 1·WUXI XINDA MEDICAL DEVICE CO., LTD·Registered Mar 28, 2007 – Mar 28, 2012CancelledRegistration details
- Analysis ID
- 9f3e67183273c123d6d324c10c2e321b
- Customs Code
- DHA04600035701
Company information
- Manufacturer
- WUXI XINDA MEDICAL DEVICE CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- HEALTH & LIFE 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
- import
Dates and status
- Registration Date
- Mar 28, 2007
- Expiry Date
- Mar 28, 2012
- Cancellation Date
- Jul 25, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Ruikang blood collection pen and blood lancet needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9f3e67183273c123d6d324c10c2e321b and manufactured by WUXI XINDA MEDICAL DEVICE CO., LTD. The authorized representative in Taiwan is HEALTH & LIFE CO., LTD..
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