Taiwan FDA registration 47481624cf9e39aedd9e25b5771cc1b8

"Bidanriki" manual instrument for general surgery (not sterilized)

TW: “美敦力” 一般手術用手動式器械 (未滅菌)

Taiwan·Risk Class 1·MEDTRONIC SOFAMOR DANEK USA, INC.·Registered Aug 31, 2009 – Aug 31, 2029Active

Registration details

Analysis ID: 47481624cf9e39aedd9e25b5771cc1b8
Customs Code: DHA04400802000

Company information

Manufacturer: MEDTRONIC SOFAMOR DANEK USA, INC.
Manufacturer Country: United States
Authorized Representative: MEDTRONIC (TAIWAN) 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: Aug 31, 2009
Expiry Date: Aug 31, 2029

About this record

Access comprehensive regulatory information for "Bidanriki" manual instrument for general surgery (not sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 47481624cf9e39aedd9e25b5771cc1b8 and manufactured by MEDTRONIC SOFAMOR DANEK USA, INC.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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