Taiwan FDA registration cfd34a8b24a4383dca5edfdb3389f82c

"Medtronic" Edmiro paclitaxel coated peripheral balloon catheter

TW: “美敦力”愛德米羅紫杉醇塗藥周邊球囊導管

Taiwan·Risk Class 2·Medtronic Inc.;; MEDTRONIC IRELAND·Registered Jan 21, 2013 – Jan 21, 2028Active

Registration details

Analysis ID: cfd34a8b24a4383dca5edfdb3389f82c
Customs Code: DHA00602452301

Company information

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

Product details

Intended Use: Details such as the Chinese imitation single approved version of the performance change: details such as the approved Chinese instruction manual (the original approved label, instruction manual or packaging on September 30, 106 will be recycled and invalidated).
Product Type (Level 1): E Cardiovascular Medicine Science
Product Type (Level 2): E.1250 Percutaneous catheters
Import Information: import

Dates and status

Registration Date: Jan 21, 2013
Expiry Date: Jan 21, 2028

About this record

Access comprehensive regulatory information for "Medtronic" Edmiro paclitaxel coated peripheral balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cfd34a8b24a4383dca5edfdb3389f82c and manufactured by Medtronic Inc.;; MEDTRONIC IRELAND. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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