Taiwan FDA registration bbb9020f52d0b8469ff59db574139717
Jiameng microlancet (sterilized)
TW: 佳盟微量採血針(滅菌)
Taiwan·Risk Class 1·SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.·Registered Aug 24, 2009 – Aug 24, 2024ExpiredRegistration details
- Analysis ID
- bbb9020f52d0b8469ff59db574139717
- Customs Code
- DHA04600075905
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
- Chinese goods;; input
Dates and status
- Registration Date
- Aug 24, 2009
- Expiry Date
- Aug 24, 2024
About this record
Access comprehensive regulatory information for Jiameng microlancet (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bbb9020f52d0b8469ff59db574139717 and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is Aksotek Company.
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