Taiwan FDA registration 828f4738a6a175b65a72591037859c77

"Keisei" Manual instrument for general surgery (sterile/unsterilized)

TW: "京成" 一般手術用手動式器械 (滅菌/未滅菌)

Taiwan·Risk Class 1·KEISEI MEDICAL INDUSTRIAL CO., LTD·Registered Nov 14, 2017 – Nov 14, 2027Active

Registration details

Analysis ID: 828f4738a6a175b65a72591037859c77
Customs Code: DHA09401850306

Company information

Manufacturer: KEISEI MEDICAL INDUSTRIAL CO., LTD
Manufacturer Country: Japan
Authorized Representative: CHIUYU MEDICAL 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: QMS/QSD;; 輸入

Dates and status

Registration Date: Nov 14, 2017
Expiry Date: Nov 14, 2027

About this record

Access comprehensive regulatory information for "Keisei" Manual instrument for general surgery (sterile/unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 828f4738a6a175b65a72591037859c77 and manufactured by KEISEI MEDICAL INDUSTRIAL CO., LTD. The authorized representative in Taiwan is CHIUYU MEDICAL CO., LTD..

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