Taiwan FDA registration fdedcfc9004e5e4ed062578b4415f318

"修弗萊迪" 派客威 Manual instrument for general surgery (unsterilized)

TW: “修弗萊迪” 派客威一般手術用手動式器械 (未滅菌)

Taiwan·Risk Class 1·Parkway Metal Products, Inc;; HU-FRIEDY MFG. CO., LLC·Registered Sep 26, 2020 – Sep 26, 2025Expired

Registration details

Analysis ID: fdedcfc9004e5e4ed062578b4415f318
Customs Code: DHA09402199600

Company information

Manufacturer: Parkway Metal Products, Inc;; HU-FRIEDY MFG. CO., LLC
Manufacturer Country: United States
Authorized Representative: YONG CHIEH ENTERPRISE 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;; Contract manufacturing

Dates and status

Registration Date: Sep 26, 2020
Expiry Date: Sep 26, 2025

About this record

Access comprehensive regulatory information for "修弗萊迪" 派客威 Manual instrument 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 fdedcfc9004e5e4ed062578b4415f318 and manufactured by Parkway Metal Products, Inc;; HU-FRIEDY MFG. CO., LLC. The authorized representative in Taiwan is YONG CHIEH ENTERPRISE CO., LTD..

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