Taiwan FDA registration 44cc659d7a9d5f5e327a87cd5c6db73f
AICA Lancet (sterilized)
TW: 愛克 採血針 (滅菌)
Taiwan·Risk Class 1·SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.·Registered Dec 21, 2018 – Dec 21, 2028ActiveRegistration details
- Analysis ID
- 44cc659d7a9d5f5e327a87cd5c6db73f
- Customs Code
- DHA09600364600
Company information
- Manufacturer Country
- China
- Authorized Representative
- TAIDOC TECHNOLOGY CORPORATION
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;; QMS/QSD;; input
Dates and status
- Registration Date
- Dec 21, 2018
- Expiry Date
- Dec 21, 2028
About this record
Access comprehensive regulatory information for AICA 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 44cc659d7a9d5f5e327a87cd5c6db73f and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is TAIDOC TECHNOLOGY CORPORATION.
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