Taiwan FDA registration d27517c0c3161c90ede2be76be08c1fc

"Medtronic" bone cement dispenser (sterilization)

TW: "美敦力" 骨水泥分配器 (滅菌)
Taiwan flagTaiwan·Risk Class 1·Medtronic Mexico S. de R.L.de CV·Registered Jan 05, 2016 – Jan 05, 2021Cancelled
Registration details
Analysis ID
d27517c0c3161c90ede2be76be08c1fc
Customs Code
DHA09401604607
Company information
Manufacturer Country
Mexico
Authorized Representative
MEDTRONIC (TAIWAN) LTD.
Product details
Intended Use
Limited to the first level identification range of the bone cement dispenser (N.4200) of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
N Orthopedics
Product Type (Level 2)
N.4200 Bone cement distributor
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Jan 05, 2016
Expiry Date
Jan 05, 2021
Cancellation Date
Oct 12, 2023
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for "Medtronic" bone cement dispenser (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d27517c0c3161c90ede2be76be08c1fc and manufactured by Medtronic Mexico S. de R.L.de CV. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MEDTRONIC SOFAMOR DANEK USA, INC., and 1 recent registrations in the same category. 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.

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