Artificial Blood Vessel - Vietnam Registration 2301555ĐKLH/BYT-HTTB

Access comprehensive regulatory information for Artificial Blood Vessel 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 2301555ĐKLH/BYT-HTTB and manufactured by Theo theo phụ lục.

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including LeMaitre Vascular, Inc. , Aesculap Chifa Sp. z o. o., 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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2301555ĐKLH/BYT-HTTB

Registration Details

Vietnam MOH Registration: 2301555ĐKLH/BYT-HTTB

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Device Details

Artificial Blood Vessel

VN: Mạch máu nhân tạo

Risk Class TTBYT Loại D

Registration Details

Analysis ID

2301555ĐKLH/BYT-HTTB

Submission ID

000.00.04.G18-210707-0006

Product Type

Theo theo phụ lục

Product Code

Theo phụ lục

Technical Details

Intended Use

The INTERGARD synthetic graft is indicated for surgical repair, bridging, or replacement of arteries in the treatment of aneurysm and occlusion of the abdominal aorta, visceral arteries, and peripheral arteries. Due to its low permeability, these products are recommended for use in patients who require heparinization prior to or during surgery.