Taiwan FDA registration 212ea7e83ab5b139470dc9915054b3ae

"Medtronic" pediatric cannula with arterial root

TW: “美敦力”小兒用動脈根部套管
Taiwan flagTaiwan·Risk Class 2·Medtronic Perfusion Systems;; Medtronic Inc.·Registered Dec 24, 2008 – Dec 24, 2028Active
Registration details
Analysis ID
212ea7e83ab5b139470dc9915054b3ae
Customs Code
DHA00601952508
Company information
Manufacturer Country
United States
Authorized Representative
MEDTRONIC (TAIWAN) LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
E Cardiovascular Medicine Science
Product Type (Level 2)
E.4210 Vascular catheters, cannulas and tubes for cardiopulmonary vascular bypassing
Import Information
import
Dates and status
Registration Date
Dec 24, 2008
Expiry Date
Dec 24, 2028
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About this record

Access comprehensive regulatory information for "Medtronic" pediatric cannula with arterial root in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 212ea7e83ab5b139470dc9915054b3ae and manufactured by Medtronic Perfusion Systems;; Medtronic Inc.. 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 PERFUSION SYSTEMS, 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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