Taiwan FDA registration 73a1eb5dfda7a46737e88fefd0181428

Medtronic Cement Dispenser (Dead/Unkilled)

TW: "美敦力" 骨水泥分配器(滅菌/未滅菌)

Taiwan·Risk Class 1·MEDTRONIC SOFAMOR DANEK USA, INC.·Registered Mar 25, 2024 – Mar 25, 2029Active

Registration details

Analysis ID: 73a1eb5dfda7a46737e88fefd0181428
Customs Code: DHA09402343203

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 "Bone Cement Dispenser (N.4200)" for the classification and grading management measures of medical equipment.
Product Type (Level 1): N Orthopedics
Product Type (Level 2): N.4200 Bone cement distributor
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Mar 25, 2024
Expiry Date: Mar 25, 2029

About this record

Access comprehensive regulatory information for Medtronic Cement Dispenser (Dead/Unkilled) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 73a1eb5dfda7a46737e88fefd0181428 and manufactured by MEDTRONIC SOFAMOR DANEK USA, INC.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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