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“Angiomed”LifeStent 5F Vascular Stent System - Taiwan Registration 2f8a190ec9912cb17eb90132438d0017

Access comprehensive regulatory information for “Angiomed”LifeStent 5F Vascular 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 2f8a190ec9912cb17eb90132438d0017 and manufactured by ANGIOMED GMBH & CO. MEDIZINTECHNIK KG. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..

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2f8a190ec9912cb17eb90132438d0017
Registration Details
Taiwan FDA Registration: 2f8a190ec9912cb17eb90132438d0017
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Device Details

“Angiomed”LifeStent 5F Vascular Stent System
TW: “安吉美爾德”萊弗史丹血管支架系統
Risk Class 2
MD

Registration Details

2f8a190ec9912cb17eb90132438d0017

Ministry of Health Medical Device Import No. 036335

DHA05603633506

Company Information

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E0001 Cardiovascular stents

Imported from abroad

Dates and Status

Mar 27, 2023

Mar 27, 2028