Ventricular Arrhythmia
- Analysis ID
- 2402671ĐKLH/BYT-HTTB
- Submission ID
- 000.00.04.G18-230313-0003
- Product Type
- Theo theo phụ lục
- Product Code
- Theo phụ lục
- Manufacturer
- Conic Vascular Technology, S.A.
- Manufacturer Country
- Theo theo phụ lục
- Product Owner
- Conic Vascular Technology, S.A.
- Authorized Representative
- CÔNG TY TNHH DƯỢC PHẨM VÀ THIẾT BỊ Y TẾ LONG BÌNH
- Intended Use
- OBJECTIVE: The clinical data currently available indicate that the lumen diameter of the coronary artery at the location of certain types of stenosis can increase due to the expansion of the balloon and PTCA is a safe and effective procedure to reduce some forms of coronary artery disease caused by atherosclerosis (see Indications). INDICATIONS: PTCA (percutaneous transluminal coronary angioplasty) may be indicated by the physician for patients with severe coronary artery disease who are candidates for coronary artery bypass surgery and who meet one of the following selection criteria: 1. The patient has atherosclerotic coronary artery disease that is amenable to balloon dilation. 2. The patient has atherosclerotic disease of the native coronary arteries and/or a coronary artery bypass graft and has recurrent symptoms and (a) progressive disease or (b) narrowing and occlusion of the graft
- Registration Date
- Oct 02, 2024
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Access comprehensive regulatory information for Ventricular Arrhythmia 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 2402671ĐKLH/BYT-HTTB and manufactured by Conic Vascular Technology, S.A.. The authorized representative in Vietnam is CÔNG TY TNHH DƯỢC PHẨM VÀ THIẾT BỊ Y TẾ LONG BÌNH.
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