Taiwan FDA registration 727073530f2a5fd572c1013df4daeac6

Medtronic Thunderbolt Pneumatic High Speed System Accessories (Sterilization)

TW: 〝美敦力〞雷勁氣壓式高速系統附件 (滅菌)

Taiwan·Risk Class 1·MEDTRONIC POWERED SURGICAL SOLUTIONS·Registered Oct 20, 2005 – Oct 20, 2015Cancelled

Registration details

Analysis ID: 727073530f2a5fd572c1013df4daeac6
Customs Code: DHA04400112008

Company information

Manufacturer: MEDTRONIC POWERED SURGICAL SOLUTIONS
Manufacturer Country: United States
Authorized Representative: MEDTRONIC (TAIWAN) LTD.

Product details

Intended Use: It is used to provide electricity during surgery to operate various accessories or accessories to cut hard or bone and soft tissues.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4820 Surgical Appliances and Accessories or Accessories
Import Information: import

Dates and status

Registration Date: Oct 20, 2005
Expiry Date: Oct 20, 2015
Cancellation Date: Apr 25, 2018

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for Medtronic Thunderbolt Pneumatic High Speed System Accessories (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 727073530f2a5fd572c1013df4daeac6 and manufactured by MEDTRONIC POWERED SURGICAL SOLUTIONS. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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