Taiwan FDA registration fda8c638450720c6384002eb9947e802
"AXA" blood lancet (sterilized)
TW: "安盛" 採血針(滅菌)
Taiwan·Risk Class 1·TIANJIN HUAHONG TECHNOLOGY CO., LTD.·Registered Nov 02, 2015 – Nov 02, 2020CancelledRegistration details
- Analysis ID
- fda8c638450720c6384002eb9947e802
- Customs Code
- DHA09600253907
Company information
- Manufacturer
- TIANJIN HUAHONG TECHNOLOGY CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- IXENSOR 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;; QMS/QSD
Dates and status
- Registration Date
- Nov 02, 2015
- Expiry Date
- Nov 02, 2020
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "AXA" blood lancet (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fda8c638450720c6384002eb9947e802 and manufactured by TIANJIN HUAHONG TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is IXENSOR CO., LTD..
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