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Aortic Root Stent Frame Accompanied by a Segment of Artificial Coronary Artery - Vietnam Registration 2402838ĐKLH/BYT-HTTB

Access comprehensive regulatory information for Aortic Root Stent Frame Accompanied by a Segment of Artificial Coronary Artery in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại D medical device is registered under number 2402838ĐKLH/BYT-HTTB and manufactured by Vascutek Limited. The authorized representative in Vietnam is CÔNG TY TNHH THIẾT BỊ Y TẾ TERUMO VIỆT NAM.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 300,000+ Vietnamese medical device registrations, helping global MedTech companies navigate Vietnam MOH regulations, identify competitors, and discover partnership opportunities efficiently.

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2402838ĐKLH/BYT-HTTB
Registration Details
Vietnam MOH Registration: 2402838ĐKLH/BYT-HTTB
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Device Details

Aortic Root Stent Frame Accompanied by a Segment of Artificial Coronary Artery
VN: Khung giá đỡ động mạch chủ ngực kèm đoạn mạch máu nhân tạo quai động mạch chủ
Risk Class TTBYT Loại D

Registration Details

2402838ĐKLH/BYT-HTTB

000.00.04.G18-230912-0006

Theo theo phụ lục

Theo phụ lục

Company Information

Theo theo phụ lục

Vascutek Limited

Technical Details

The purpose of Thoraflex Hybrid is to treat aortic aneurysm and/or dissection of the aorta and its branches, which may or may not involve the ascending aorta, by open surgery to reduce the risk of aortic rupture and death related to the aorta.

Dates and Status

Oct 22, 2024