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Angioplasty guidewires used in cardiac intervention - Vietnam Registration 2402022ĐKLH/BYT-HTTB

Access comprehensive regulatory information for Angioplasty guidewires used in cardiac intervention 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 2402022ĐKLH/BYT-HTTB and manufactured by Abbott Medical. The authorized representative in Vietnam is CÔNG TY TNHH THIẾT BỊ Y TẾ KHẢI VINH.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Theo theo phụ lục, and 2 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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2402022ĐKLH/BYT-HTTB
Registration Details
Vietnam MOH Registration: 2402022ĐKLH/BYT-HTTB
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Device Details

Angioplasty guidewires used in cardiac intervention
VN: Dụng cụ mở đường vào mạch máu dùng trong can thiệp tim mạch
Risk Class TTBYT Loại D

Registration Details

2402022ĐKLH/BYT-HTTB

000.00.04.G18-231222-0007

Theo theo phụ lục

Theo phụ lục

Company Information

Theo theo phụ lục

Abbott Medical

Technical Details

The vascular access devices used in cardiac surgical procedures are intended to provide a route into the venous circulation to deliver cardiac pacing wires and catheters into the venous vascular system of patients who are designated to use cardiac rhythm control devices to treat heart failure, arrhythmia, or abnormal heart conduction.

Dates and Status

Aug 27, 2024

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