Subarachnoid Space Support Frame - Vietnam Registration 2403356ĐKLH/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 2403356ĐKLH/BYT-HTTB and manufactured by ev3, Inc.. The authorized representative in Vietnam is CÔNG TY TNHH MEDTRONIC VIỆT NAM.
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Device Details
Registration Details
2403356ĐKLH/BYT-HTTB
000.00.04.G18-231123-0019
Theo theo phụ lục
Theo phụ lục
Technical Details
1. Peripheral: The stent is indicated for use in the following types of occlusions or injuries: • High-risk occlusions or injuries that are at risk of sudden closure or re-occlusion after percutaneous transluminal coronary angioplasty (PTCA) • High-risk occlusions or injuries that are at risk of re-occlusion after PTCA in the iliac arteries, common iliac arteries, or femoral arteries The stent is intended to be placed to improve and maintain the diameter of the artery. 2. Intraluminal: The stent is indicated for the treatment of common carotid artery (CCA), internal carotid artery (ICA), and carotid artery branch stenosis.
Dates and Status
Nov 06, 2024