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Magnetic Resonance Imaging System - Vietnam Registration 240003158/PCBB-HN

Access comprehensive regulatory information for Magnetic Resonance Imaging System in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TBYT Loại B medical device is registered under number 240003158/PCBB-HN and manufactured by GE Healthcare Manufacturing LLC. The authorized representative in Vietnam is CÔNG TY TNHH GE HEALTHCARE VIỆT NAM.

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including Siemens Healthcare GmbH, GE Healthcare Manufacturing LLC, and 5 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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240003158/PCBB-HN
Registration Details
Vietnam MOH Registration: 240003158/PCBB-HN
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Device Details

Magnetic Resonance Imaging System
VN: Hệ thống chụp cộng hưởng từ
Risk Class TBYT Loại B

Registration Details

240003158/PCBB-HN

000.00.19.H26-241021-0006

SIGNA Victor

Company Information

GE Healthcare (Tianjin) Company Limited

Technical Details

The SIGNA™ Victor system is a whole-body MRI scanner used to create images of the inside of the human body, aiding in diagnosis. In clinical practice, MRI can be used to differentiate diseased or damaged tissue from normal tissue. MRI technology is commonly used to help diagnose conditions such as cancer, stroke, heart disease and peripheral vascular disease, pediatric disorders, and more. However, MRI technology, in general, is not limited to specific diseases, stages, and conditions of the disease, or clinical subtypes. The MRI technology is intended to be used by healthcare professionals (clinical doctors and trained technologists) after good clinical practice. This technology can be used for many patient populations, including adults, children, and neonates, in accordance with good clinical practice.

Dates and Status

Nov 18, 2024