Vietnam MOH registration 2403040ĐKLH/BYT-HTTB

Peripheral Vascular Support Frame

VN: Khung giá đỡ mạch ngoại vi
Vietnam flagVietnam·Risk Class TTBYT Loại C·Theo theo phụ lục·Registered Nov 02, 2024
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
Company information
Authorized Representative
CÔNG TY TNHH MERIL (VIỆT NAM)
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.
Dates and status
Registration Date
Nov 02, 2024
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About this record

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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