Taiwan FDA registration 71ffc41106477bbe46eef6af0a818260

Arterial cannula

TW: 動脈套管
Taiwan flagTaiwan·Risk Class 2·Medtronic Perfusion Systems;; Medtronic Inc.·Registered Oct 31, 1998 – Oct 31, 2028Active
Registration details
Analysis ID
71ffc41106477bbe46eef6af0a818260
Customs Code
DHA00600891102
Company information
Manufacturer Country
United States
Authorized Representative
MEDTRONIC (TAIWAN) LTD.
Product details
Product Type (Level 1)
0699 Other Intensive Care Unit & Cardiac Care Unit Equipment
Import Information
import
Dates and status
Registration Date
Oct 31, 1998
Expiry Date
Oct 31, 2028
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About this record

Access comprehensive regulatory information for Arterial cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 71ffc41106477bbe46eef6af0a818260 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, 4 companies making similar products including Medtronic Perfusion Systems;; Medtronic Inc., MEDTRONIC CARDIAC SURGICAL PRODUCTS, and 5 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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