Philips innovative MR 5300 magnetic resonance imaging system simplifies and automates the most complex clinical and operational tasks. So you can create highly personalized exams of even your most challenging patients. Quickly. Easily. Intelligently. Smart Workflow reduces the number of steps needed to complete an MR exam and enables guided patient set-up in under a minute, the ultra-lightweight and flexible Breeze coils help cut patient change-over time by 30% to keep your MR department on schedule. At the same time, they improve patient comfort and staff satisfaction. This will help you meeting the challenging demands of productivity and patient throughput at private clinics and diagnostic imaging centers. MR 5300 is not only a fast MR, but also smart and flexible, providing intelligent tools for fast exams and quality scanning.

Philips innovative MR 5300 magnetic resonance imaging system simplifies and automates the most complex clinical and operational tasks. So you can create highly personalized exams of even your most challenging patients. Quickly. Easily. Intelligently. Smart Workflow reduces the number of steps needed to complete an MR exam and enables guided patient set
MR 5000 Series - MR 5300

A diagnostic general-purpose magnetic resonance imaging (MRI) system designed to scan any targeted area of the body (full-body imaging). This system includes a superconducting magnet assembly and can be fixed-location, mobile, or transportable. Some systems can perform MR spectroscopy or various real-time imaging procedures for MRI guided interventional, therapeutic, or surgical applications. The system is available in a variety of system gantry configurations including closed bore, open bore, and open-sided or other kinds of patient accessible designs.

No Data Available

Device Sterile: False

Sterilization Prior To Use: False

Sterilization Methods: No Data Available

Code: LNH

Device Name: System, Nuclear Magnetic Resonance Imaging

Device Class: 2

Physical State: N/A

Definition: N/A

Submission Type ID: 1

Review Panel: RA

Review Code: N/A

Technical Method: N

Gmp Exempt Flag: N/A

Life Sustain Support Flag: N

Unclassified Reason: N/A

Implant Flag: N

Target Area: N/A

Regulation Number: 892.1000

Third Party Flag: Y

Medical Specialty: RA

Device Id: 00884838112841

Device Type: Primary

DeviceId Issuing Agency: GS1

Contains DI Number: N/A

Package Quantity: N/A

Package Discontinue Date: N/A

Package Status: N/A

Package Type: N/A