Taiwan FDA registration e0678051b0725e624abc8dff4224b6a4

"Dunfer" manual instruments for general surgery (unsterilized)

TW: "登弗"一般手術用手動式器械(未滅菌)

Taiwan·Risk Class 1·DUFNER INSTRUMENTE GMBH·Registered May 02, 2006 – May 02, 2026Expired

Registration details

Analysis ID: e0678051b0725e624abc8dff4224b6a4
Customs Code: DHA04400430601

Company information

Manufacturer: DUFNER INSTRUMENTE GMBH
Manufacturer Country: Germany
Authorized Representative: GOLDENSPRING MEDI-TECH 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: May 02, 2006
Expiry Date: May 02, 2026

About this record

Access comprehensive regulatory information for "Dunfer" 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 e0678051b0725e624abc8dff4224b6a4 and manufactured by DUFNER INSTRUMENTE GMBH. The authorized representative in Taiwan is GOLDENSPRING MEDI-TECH CO., LTD..

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