Peripheral Vascular Support Frame - Vietnam Registration 2403040ĐKLH/BYT-HTTB

Access comprehensive regulatory information for Peripheral Vascular Support Frame in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại C medical device is registered under number 2403040ĐKLH/BYT-HTTB. The authorized representative in Vietnam is CÔNG TY TNHH MERIL (VIỆT NAM).

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Angiomed GmbH & Co. Medizintechnik, Angiomed GmbH & Co. Medizintechnik, and 4 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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2403040ĐKLH/BYT-HTTB

Registration Details

Vietnam MOH Registration: 2403040ĐKLH/BYT-HTTB

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Device Details

Peripheral Vascular Support Frame

VN: Khung giá đỡ mạch ngoại vi

Risk Class TTBYT Loại C

Registration Details

Analysis ID

2403040ĐKLH/BYT-HTTB

Submission ID

000.00.04.G18-231218-0047

Product Type

Theo theo phụ lục

Product Code

Theo phụ lục

Technical Details

Intended Use

Promesa BMS - The Nitinol self-expanding stent system is designed for the treatment of peripheral artery diseases with reference vessel diameters ranging from 5.00 mm to 7.00 mm for Femoral Artery Occlusion (FAS) and 7.00 mm to 10.00 mm for Iliac and Aortoiliac arteries in patients who are candidates for percutaneous transluminal angioplasty (PTA) and stent placement.