Taiwan FDA registration 4dcf357dc81310f94e2bee5428038843
Jiameng micro blood collection pen (unsterilized)
TW: 佳盟微量採血筆(未滅菌)
Taiwan·Risk Class 1·SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.·Registered Aug 24, 2009 – Aug 24, 2024ExpiredRegistration details
- Analysis ID
- 4dcf357dc81310f94e2bee5428038843
- Customs Code
- DHA04600076003
Company information
- Manufacturer Country
- China
- Authorized Representative
- Aksotek Company
Product details
- Intended Use
- Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
- 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
- Aug 24, 2009
- Expiry Date
- Aug 24, 2024
About this record
Access comprehensive regulatory information for Jiameng micro blood collection pen (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4dcf357dc81310f94e2bee5428038843 and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is Aksotek Company.
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