Taiwan FDA registration 0a0934bc91363d44ec6362845e839ecb

"Medtronic" Foramen catheter for the left ventricle

TW: "美敦力" 左心室用孔狀導管

Taiwan·Risk Class 2·Medtronic Inc.;; MEDTRONIC PERFUSION SYSTEMS·Registered Oct 17, 2002 – Oct 17, 2027Active

Registration details

Analysis ID: 0a0934bc91363d44ec6362845e839ecb
Customs Code: DHA00601011305

Company information

Manufacturer: Medtronic Inc.;; MEDTRONIC PERFUSION SYSTEMS
Manufacturer Country: United States
Authorized Representative: MEDTRONIC (TAIWAN) LTD.

Product details

Intended Use: Vacuum.
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: Oct 17, 2002
Expiry Date: Oct 17, 2027

About this record

Access comprehensive regulatory information for "Medtronic" Foramen catheter for the left ventricle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0a0934bc91363d44ec6362845e839ecb and manufactured by Medtronic Inc.;; MEDTRONIC PERFUSION SYSTEMS. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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