Full Body 0.3 Tesla Permanent Magnet MRI System

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Part Number: BTI-030

Availability: Contact us for pricing

Feature: Certification: CE, ISO13485

Feature: Model No. BTI-030

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Description

Full Body 0.3 Tesla Permanent Magnet MRI System

Gap: Large - Open

Application: Whole Body

Dynamic Range: =80dB

Magnet System

Magnet Type: Permanent magnet with automatic constant temperature system

1.2 Field strength 0.3T

1.3 Magnet shape C-shape

1.4 Homogeneity (40cm, DSV, VRMS) =2.5ppm

1.5 Shim method Active/Passive/Dynamic

1.6 Magnet vertical gap 40cm

1.7 Accessibility (Horizontal opening angle) >250°

1.8 5 Gauss fringe field 2.5m*2.5m*2.5m

Gradient System

2.1 Gradient field strength (Single Axis) 25mT/m

2.2 Gradient slew rate (Single Axis) 75mT/m/ms

2.3 Rise time 0.3ms

2.4 Gradient cooling system(Gradient coils and power electronics) Air

With Mature, clinically available solutions that meet U.S. healthcare standards, we’re able to provide a full lineup of CE Certified MRI (Magnetic Resonance Imaging) systems - A core product category of ours with proven performance, global regulatory compliance, and broad applicability to U.S. hospitals, diagnostic centers, and clinics.

Why Our CE-Certified MRI Systems Are a Strong Fit for U.S. Healthcare Needs:

Our MRI product line is engineered to address diverse clinical requirements (neurology, oncology, musculoskeletal, obstetrics) while complying with strict international standards as well; including CE Class II certification (aligned with EU Medical Device Regulation (MDR)) and ISO 13485 quality management certification. For the U.S. market, our MRI systems also meet key operational needs: non-invasive imaging (no ionizing radiation), compatibility with U.S. PACS/RIS platforms, and support for low-dose protocols (critical for pediatric and repeated exams).

Support for your team evaluation:
To help your team explore our MRI solutions further, feel free to request any customized materials for your project. We will send a MRI product brochure (including CE certification copies, FDA readiness documents, and clinical case studies from U.S. partner facilities).

We’ll discuss and help handle any site constraints (space, power) or regulatory priorities (e.g., FDA 510(k) support timeline).
Virtual Demo & Q&A: Upon request, we can arrange a live virtual demo (led by our U.S. based technical team) to walk you through the entire system operation, software integration, and post-sales support.

We understand that shifting from CT to MRI requires careful evaluation and our CE-certified MRI line offers a mature, regulatory-compliant alternative that enhances diagnostic capabilities for U.S. patients. Please feel free to reply with your preferences, and we’ll respond promptly to move our cooperation forward.

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