Artificial Heart Valve - Vietnam Registration 2403371ĐKLH/BYT-HTTB

Access comprehensive regulatory information for Artificial Heart Valve 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 2403371ĐKLH/BYT-HTTB and manufactured by Medtronic Plc. The authorized representative in Vietnam is CÔNG TY TNHH MEDTRONIC VIỆT NAM.

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including Medtronic Heart Valves Division; Medtronic Mexico S. de R.L de CV, Edwards Lifesciences LLC; Edwards Lifesciences (Singapore) Pte Ltd, and 5 recent registrations in the same category. 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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2403371ĐKLH/BYT-HTTB

Registration Details

Vietnam MOH Registration: 2403371ĐKLH/BYT-HTTB

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Device Details

Artificial Heart Valve

VN: Vòng van tim nhân tạo

Risk Class TTBYT Loại D

Registration Details

Analysis ID

2403371ĐKLH/BYT-HTTB

Submission ID

17000440/ĐKLH-BYT-TB-CT

Product Type

Theo theo phụ lục

Product Code

Theo phụ lục

Technical Details

Intended Use

The Duran AnCore artificial heart valve is indicated for the re-structuring or repair of diseased bicuspid and tricuspid valves. Appropriate treatment and repair of the valve annulus can correct both valve regurgitation and stenosis. Note: The functionality of the Duran AnCore artificial heart valve's chordal guidance feature is indicated only for the surgical repair of the diseased bicuspid valve.