Taiwan FDA registration 5fb56299dcf06e673661927735743e35

"Freda" manual instruments for general surgery (unsterilized)

TW: “富瑞達”一般手術用手動式器械 (未滅菌)

Taiwan·Risk Class 1·FUJITA MEDICAL INSTRUMENTS CO., LTD.·Registered Jul 06, 2006 – Jul 06, 2026Expired

Registration details

Analysis ID: 5fb56299dcf06e673661927735743e35
Customs Code: DHA04400487205

Company information

Manufacturer: FUJITA MEDICAL INSTRUMENTS CO., LTD.
Manufacturer Country: Japan
Authorized Representative: WELLONG INSTRUMENTS 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: import

Dates and status

Registration Date: Jul 06, 2006
Expiry Date: Jul 06, 2026

About this record

Access comprehensive regulatory information for "Freda" manual instruments for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5fb56299dcf06e673661927735743e35 and manufactured by FUJITA MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is WELLONG INSTRUMENTS CO., LTD..

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