Taiwan FDA registration 5005dc3df6bd7bba2b665b069d8f998d
Xiamen Dingjing blood collection pen
TW: 廈門鼎晶採血筆
Taiwan·Risk Class 1·XIAMEN DINGJING PLASTIC CO., LTD.·Registered Dec 24, 2010 – Dec 24, 2015CancelledRegistration details
- Analysis ID
- 5005dc3df6bd7bba2b665b069d8f998d
- Customs Code
- DHA04600121509
Company information
- Manufacturer
- XIAMEN DINGJING PLASTIC CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- Taiwan Nipro Medical Device 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
- Input;; Chinese goods
Dates and status
- Registration Date
- Dec 24, 2010
- Expiry Date
- Dec 24, 2015
- Cancellation Date
- May 10, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Xiamen Dingjing blood collection pen in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5005dc3df6bd7bba2b665b069d8f998d and manufactured by XIAMEN DINGJING PLASTIC CO., LTD.. The authorized representative in Taiwan is Taiwan Nipro Medical Device Co., Ltd.
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