Taiwan FDA registration 9ab26f896462ebcef773ca3f1af7ab63

"Bidanriki" Manual instrument for general surgery (sterilization)

TW: “美敦力” 一般手術用手動式器械 (滅菌)

Taiwan·Risk Class 1·Medtronic Perfusion Systems;; Medtronic Inc.·Registered Dec 07, 2012 – Dec 07, 2027Cancelled

Registration details

Analysis ID: 9ab26f896462ebcef773ca3f1af7ab63
Customs Code: DHA04401245307

Company information

Manufacturer: Medtronic Perfusion Systems;; Medtronic Inc.
Manufacturer Country: United States
Authorized Representative: MEDTRONIC (TAIWAN) LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Dec 07, 2012
Expiry Date: Dec 07, 2027
Cancellation Date: Sep 13, 2022

Cancellation information

Status: Logged out
Reason: 自請註銷

About this record

Access comprehensive regulatory information for "Bidanriki" Manual instrument for general surgery (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9ab26f896462ebcef773ca3f1af7ab63 and manufactured by Medtronic Perfusion Systems;; Medtronic Inc.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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