"Medtronic" Clinical Bone Cement Mixer (Sterilization) - Taiwan Registration 3f7bd40f4dc626b674705852f24ed4d9
Access comprehensive regulatory information for "Medtronic" Clinical Bone Cement Mixer (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3f7bd40f4dc626b674705852f24ed4d9 and manufactured by MEDTRONIC SOFAMOR DANEK USA, INC.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Product Details
Limited to the first level identification range of the "Clinical Bone Cement Mixer (N.4210)" of the Measures for the Classification and Grading Management of Medical Equipment.
N Orthopedics
N.4210 ่จๅบ็จ้ชจๆฐดๆณฅๆชๆๅจ
QMS/QSD;; ่ผธๅ ฅ
Dates and Status
Nov 16, 2021
Nov 16, 2026