Taiwan FDA registration 55a4056d01e76e0bde94bb1e80499375

"Medtronic" Enray aortic stent system

TW: “美敦力”安瑞主動脈支架系統
Taiwan flagTaiwan·Risk Class 2·MEDTRONIC VASCULAR·Registered Nov 26, 2009 – Nov 26, 2014Cancelled
Registration details
Analysis ID
55a4056d01e76e0bde94bb1e80499375
Customs Code
DHA00602044102
Company information
Manufacturer
MEDTRONIC VASCULAR
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.0001 Cardiovascular stents
Import Information
import
Dates and status
Registration Date
Nov 26, 2009
Expiry Date
Nov 26, 2014
Cancellation Date
Apr 25, 2018
Cancellation information
Status
Logged out
Reason
自行鍵入
Companies making similar products

Top companies providing products similar to ""Medtronic" Enray aortic stent system"

Recent registrations

Recently registered similar products

About this record

Access comprehensive regulatory information for "Medtronic" Enray aortic stent system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 55a4056d01e76e0bde94bb1e80499375 and manufactured by MEDTRONIC VASCULAR. 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 VASCULAR, 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.

Free DatabasePowered by Pure Global AI89,000+ Devices1 Competitors1 Recent Registrations