• News
  • Contact Us

MRI Compatibility Testing

Overview


Exponent performs magnetic resonance imaging (MRI) compatibility testing of medical devices. Through our A2LA-accredited laboratory we assist medical device manufacturers in validating MRI safety and compatibility design requirements and regulatory labeling requirements.

We have performed MRI testing on a variety of implantable devices including cardiovascular devices, spinal fixtures, endovascular coils, anchors, and orthopedic devices. We have also tested non-implantable medical devices designed to be used within the MRI environment. We provide analysis and guidance to clients with regard to FDA submission in the context of performance to standards. Exponent’s analytical techniques allow manufacturers to determine the risks associated with already-implanted devices and to formulate a strategy for serving the needs of users and patients. We have tested a number of devices which have exhibited localized radiofrequency heating, and others which have exhibited substantial displacement and torque effects. Exponent provides analysis and labeling guidelines for use in formulating a strategy for marketing the devices and to guide submissions to regulatory authorities. We also assist manufacturers with failure analysis when needed, including investigation of injuries in the MRI environment.

We have the capability—and are accredited to ISO 17025—to test at 1.5T and 3.0T with both wide-bore and conventional-bore configurations in accordance with all applicable ASTM standards (listed below). Exponent also has arrangements with regional research institutions to conduct studies at high field strength, if needed.

Standards

ASTM F2052 – Standard Test Method for Measurement of Magnetically Induced Displacement Force on Medical Devices in the Magnetic Resonance Environment

ASTM F2119 – Standard Test Method for Evaluation of MR Image Artifacts from Passive Implants

ASTM F2182 – Standard Test Method for Measurement of Radio Frequency Induced Heating Near Passive Implants During Magnetic Resonance Imaging

ASTM F2213 – Standard Test Method for Measurement of Magnetically Induced Torque on Medical Devices in the Magnetic Resonance Environment

Medical Devices of Interest for Interaction with Magnetic Resonance

  • Neurointerventional devices: aneurysm clips and coils, hydrocephalus valves/shunts, neurostimulators
  • Vascular implants: stents, valves, filters Interventional instruments: catheters, guidewires, endoscopes
  • Orthopaedic/spinal devices: joint prostheses, fracture fixation hardware, fusion and deformity constructs
  • Medical monitoring and support equipment; ventilators, pumps
  • Electrophysiology devices: pacemakers, implantable cardioverter defibrillators
  • Others: handheld surgical instruments, implantable (cochlear) hearing devices

Figure 1.  Sample under test per ASTM 2119 to determine artifact size

Figure 2.  Siemens 3T MRI

Figure 3.  ASTM F2182 Phantom used to characterize radiofrequency-induced heating