Taiwan FDA registration d2bf35afb10ee11b089c7ed4b3bff19a
Ruxi Safety Lancet (Sterilization)
TW: “如禧”安全採血針 (滅菌)
Registration details
- Analysis ID
- d2bf35afb10ee11b089c7ed4b3bff19a
- Customs Code
- DHA09600356704
Company information
- Manufacturer
- Yangzhou Medline Industry Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- EAFAN ENTERPRISE CO., LTD.
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;; QMS/QSD
Dates and status
- Registration Date
- Sep 28, 2018
- Expiry Date
- Sep 28, 2028
About this record
Access comprehensive regulatory information for Ruxi Safety Lancet (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d2bf35afb10ee11b089c7ed4b3bff19a and manufactured by Yangzhou Medline Industry Co., Ltd.. The authorized representative in Taiwan is EAFAN ENTERPRISE CO., LTD..
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