Subarachnoid Space Support Frame - Vietnam Registration 2301035ĐKLH/BYT-HTTB
Access comprehensive regulatory information for Subarachnoid Space Support Frame 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 2301035ĐKLH/BYT-HTTB and manufactured by Theo theo phụ lục.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ev3, Inc., and 1 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.
Device Details
Registration Details
2301035ĐKLH/BYT-HTTB
17003185/ĐKLH-BYT-TB-CT
Theo theo phụ lục
Theo phụ lục
Technical Details
1. Peripheral: The stent is indicated for use in the following types of joints or injuries: • Sites of occlusion or high-risk stenosis that are at risk for sudden closure or re-occlusion after percutaneous transluminal angioplasty (PTA) of the coronary arteries. • High-risk stenosis that is at risk for re-occlusion after PTA in the iliac arteries, common iliac arteries, or femoral arteries. The stent is intended to improve and maintain the diameter of the artery. 2. Carotid: The stent is indicated for the treatment of common carotid artery (CCA), internal carotid artery (ICA), and carotid artery branch stenosis.
Dates and Status
Sep 28, 2023

