Taiwan FDA registration fb5885ea2f8d6eeff3512296a8391398

"Bud" Aitvans 014/018 balloon expansion catheter

TW: “巴德”艾特凡斯014/018氣球擴張導管

Taiwan·Risk Class 2·BARD PERIPHERAL VASCULAR, INC.;; CLEARSTREAM TECHNOLOGIES LTD.·Registered May 28, 2013 – May 28, 2028Active

Registration details

Analysis ID: fb5885ea2f8d6eeff3512296a8391398
Customs Code: DHA00602495807

Company information

Manufacturer: BARD PERIPHERAL VASCULAR, INC.;; CLEARSTREAM TECHNOLOGIES LTD.
Manufacturer Country: Ireland;;United States
Authorized Representative: BARD PACIFIC HEALTH CARE CO., 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.1250 Percutaneous catheters
Import Information: Contract manufacturing;; input

Dates and status

Registration Date: May 28, 2013
Expiry Date: May 28, 2028

About this record

Access comprehensive regulatory information for "Bud" Aitvans 014/018 balloon expansion catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fb5885ea2f8d6eeff3512296a8391398 and manufactured by BARD PERIPHERAL VASCULAR, INC.;; CLEARSTREAM TECHNOLOGIES LTD.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..

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