Taiwan FDA registration 986e4896d9529bd3174a19aee7cc72d3

Mr. Yoshiei Fukunaga Blood Collection Needle (Sterile)

TW: 福永宜瑪氏採血針(滅菌)

Taiwan·Risk Class 1·SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.·Registered Nov 08, 2023 – Nov 08, 2028Active

Registration details

Analysis ID: 986e4896d9529bd3174a19aee7cc72d3
Customs Code: DHA09600484103

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: QMS/QSD;; Input;; Chinese goods

Dates and status

Registration Date: Nov 08, 2023
Expiry Date: Nov 08, 2028

About this record

Access comprehensive regulatory information for Mr. Yoshiei Fukunaga Blood Collection Needle (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 986e4896d9529bd3174a19aee7cc72d3 and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is EPS BIO TECHNOLOGY CORP..

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