Taiwan FDA registration ce969c437f5cb7f32796fc53afc65c2e

Fukunaga Sane lancet (sterilization)

TW: 福永薩內採血針(滅菌)

Taiwan·Risk Class 1·SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.·Registered Nov 21, 2023 – Nov 21, 2028Active

Registration details

Analysis ID: ce969c437f5cb7f32796fc53afc65c2e
Customs Code: DHA09600484307

Company information

Manufacturer: SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.
Manufacturer Country: China
Authorized Representative: EPS BIO TECHNOLOGY CORP.

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;; QMS/QSD

Dates and status

Registration Date: Nov 21, 2023
Expiry Date: Nov 21, 2028

About this record

Access comprehensive regulatory information for Fukunaga Sane 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 ce969c437f5cb7f32796fc53afc65c2e and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is EPS BIO TECHNOLOGY CORP..

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