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“Angiomed” Bard Venovo Venous Stent System - Taiwan Registration 776bfc6689b3b03f945cc5b9e36a0a77

Access comprehensive regulatory information for “Angiomed” Bard Venovo Venous Stent System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 776bfc6689b3b03f945cc5b9e36a0a77 and manufactured by ANGIOMED GMBH & CO.MEDIZINTECHNIK KG. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..

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776bfc6689b3b03f945cc5b9e36a0a77
Registration Details
Taiwan FDA Registration: 776bfc6689b3b03f945cc5b9e36a0a77
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Device Details

“Angiomed” Bard Venovo Venous Stent System
TW: “安吉美爾德”巴德維尼弗靜脈支架系統
Risk Class 2
MD

Registration Details

776bfc6689b3b03f945cc5b9e36a0a77

Ministry of Health Medical Device Import No. 030010

DHA05603001000

Company Information

Product Details

This product is suitable for the treatment of stenosis and occlusion of the femoral vein.

E Cardiovascular devices

E0001 Cardiovascular stents

Imported from abroad

Dates and Status

Aug 14, 2017

Aug 14, 2027