Artificial Blood Vessel
Vietnam·Risk Class TTBYT Loại D·Theo theo phụ lục·Theo theo phụ lục·Registered Nov 20, 2023- Analysis ID
- 2301555ĐKLH/BYT-HTTB
- Submission ID
- 000.00.04.G18-210707-0006
- Product Type
- Theo theo phụ lục
- Product Code
- Theo phụ lục
- Manufacturer
- Theo theo phụ lục
- Manufacturer Country
- Theo theo phụ lục
- 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.
- Registration Date
- Nov 20, 2023
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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.