Taiwan FDA registration 6dff2c911de3967843b8052ff33d9081

"Xiao" General Surgery Manual Instrument (Unsterilized)

TW: "科王" 一般手術用手動式器械 (未滅菌)

Taiwan·Risk Class 1·KIRWAN SURGICAL PRODUCTS, LLC.·Registered Oct 17, 2011 – Oct 17, 2026Active

Registration details

Analysis ID: 6dff2c911de3967843b8052ff33d9081
Customs Code: DHA04401094505

Company information

Manufacturer: KIRWAN SURGICAL PRODUCTS, LLC.
Manufacturer Country: United States
Authorized Representative: BARRY TEC 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: import

Dates and status

Registration Date: Oct 17, 2011
Expiry Date: Oct 17, 2026

About this record

Access comprehensive regulatory information for "Xiao" General Surgery Manual Instrument (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6dff2c911de3967843b8052ff33d9081 and manufactured by KIRWAN SURGICAL PRODUCTS, LLC.. The authorized representative in Taiwan is BARRY TEC ENTERPRISE CO., LTD..

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