Taiwan FDA registration b1ecfe58386bb8d88c5496ae7fb20f3f
"Cinda" lancet and lancet
TW: "信達" 採血針及採血筆
Taiwan·Risk Class 1·WUXI XINDA MEDICAL DEVICE CO., LTD·Registered Mar 30, 2006 – Mar 30, 2011CancelledRegistration details
- Analysis ID
- b1ecfe58386bb8d88c5496ae7fb20f3f
- Customs Code
- DHA04600015002
Company information
- Manufacturer
- WUXI XINDA MEDICAL DEVICE CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- MIN JIER FIRM
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 30, 2006
- Expiry Date
- Mar 30, 2011
- Cancellation Date
- Jun 15, 2011
Cancellation information
- Status
- Logged out
- Reason
- 逾期展延
About this record
Access comprehensive regulatory information for "Cinda" lancet and lancet in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b1ecfe58386bb8d88c5496ae7fb20f3f and manufactured by WUXI XINDA MEDICAL DEVICE CO., LTD. The authorized representative in Taiwan is MIN JIER FIRM.
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