Taiwan FDA registration 97b30e0c167c9826482607aa5a9e71a3

Jackie Safety Lancet (Sterilized)

TW: 羅碁安全採血針 (滅菌)

Taiwan·Risk Class 1·SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.·Registered Apr 29, 2022 – Apr 29, 2027Active

Registration details

Analysis ID: 97b30e0c167c9826482607aa5a9e71a3
Customs Code: DHA09600463401

Company information

Manufacturer: SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.
Manufacturer Country: China
Authorized Representative: EBIOLOGIC TECHNOLOGY 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: Apr 29, 2022
Expiry Date: Apr 29, 2027

About this record

Access comprehensive regulatory information for Jackie Safety 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 97b30e0c167c9826482607aa5a9e71a3 and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is EBIOLOGIC TECHNOLOGY CO., LTD..

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