Taiwan FDA registration 97d455301c608842401a04fbba45d893
Gladly retractable lancet (unsterilized)
TW: 欣然可退針式採血筆(未滅菌)
Taiwan·Risk Class 1·SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.·Registered Jul 23, 2019 – Jul 23, 2029ActiveRegistration details
- Analysis ID
- 97d455301c608842401a04fbba45d893
- Customs Code
- DHA09600388607
Company information
- Manufacturer Country
- China
- Authorized Representative
- APEX BIOTECHNOLOGY 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
- Input;; QMS/QSD;; Chinese goods
Dates and status
- Registration Date
- Jul 23, 2019
- Expiry Date
- Jul 23, 2029
About this record
Access comprehensive regulatory information for Gladly retractable lancet (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 97d455301c608842401a04fbba45d893 and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is APEX BIOTECHNOLOGY CORPORATION.
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