Taiwan FDA registration f8baedfca41833963264eb8eb4d270ea

"Bud" Aitvans 035 balloon expansion catheter

TW: “巴德”艾特凡斯035氣球擴張導管

Taiwan·Risk Class 2·BARD PERIPHERAL VASCULAR, INC.;; CLEARSTREAM TECHNOLOGIES LTD.·Registered Feb 25, 2016 – Feb 25, 2026Expired

Registration details

Analysis ID: f8baedfca41833963264eb8eb4d270ea
Customs Code: DHA05602824407

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: Input;; Contract manufacturing

Dates and status

Registration Date: Feb 25, 2016
Expiry Date: Feb 25, 2026

About this record

Access comprehensive regulatory information for "Bud" Aitvans 035 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 f8baedfca41833963264eb8eb4d270ea 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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