Taiwan FDA registration 3f7bd40f4dc626b674705852f24ed4d9
"Medtronic" Clinical Bone Cement Mixer (Sterilization)
TW: "美敦力" 臨床用骨水泥攪拌器(滅菌)
Taiwan·Risk Class 1·MEDTRONIC SOFAMOR DANEK USA, INC.·Registered Nov 16, 2021 – Nov 16, 2026ActiveRegistration details
- Analysis ID
- 3f7bd40f4dc626b674705852f24ed4d9
- Customs Code
- DHA09402269902
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 range of the "Clinical Bone Cement Mixer (N.4210)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4210 臨床用骨水泥攪拌器
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Nov 16, 2021
- Expiry Date
- Nov 16, 2026
About this record
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..
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