NABL ACCREDITED · ISO/IEC 17025:2017

7 Ways We Prove Your Device Is Safe in the MR Environment

MRI Safety and Compatibility Testing for medical device implants, instruments, and accessories at our Oragadam laboratory — displacement force, torque, RF heating, image artefact, and labelling evaluation referenced to ASTM F2503 and FDA MR guidance.

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A device that behaves perfectly on the bench can still fly across the room, heat up, or vanish an entire diagnostic image the moment it enters an MRI scanner’s magnetic field.

MRI Safety and Compatibility Testing for medical device implants, surgical instruments, and patient-contact accessories answers the question a standard material study can’t: does the device stay put under a strong static field, does it heat dangerously under RF exposure, does it distort the diagnostic image around it, and is the resulting MR Conditional or MR Safe label actually backed by data. Our MRI Safety and Compatibility Testing for medical device programme at the Oragadam laboratory covers seven checkpoints across force, heating, imaging, and regulatory review, referenced to the ASTM F2503 labelling standard family and current FDA MR guidance.

FDA MR safety guidance assessment reviews the device design against the FDA’s current testing and labelling expectations for the magnetic resonance environment before any physical test begins, so the rest of the programme is scoped to exactly what a submission will need. Magnetically induced displacement testing measures the force the static field exerts on any ferromagnetic component, confirming an implant won’t shift or dislodge once a patient is positioned inside the bore, while the companion torque test measures the rotational force the field applies, since a device can pass a displacement check and still twist dangerously under the same field.

RF heating testing for medical device implants and instruments places the device inside a gel-filled phantom wired with thermocouples during a simulated MRI scan, because RF-induced heating around metal components is one of the most common real-world MR safety incidents and one a visual inspection would never catch. Image artefact testing confirms the device doesn’t obscure or distort the diagnostic image in the surrounding anatomy badly enough to compromise a radiologist’s read, and MR safety labelling testing for medical device products verifies the final MR Safe, MR Conditional, or MR Unsafe designation is fully supported by the displacement, torque, heating, and artefact data behind it. Manufacturers bring their programmes to Kiyo R&D Lab because a single missed checkpoint in Medical Device Testing doesn’t surface as a bench-test footnote — it surfaces as a dislodged implant, a burn injury, or a scan a radiologist can’t read. Running all seven checkpoints under one accredited scope at Oragadam, with reports formatted for direct regulatory submission, is what turns FDA testing for medical device MR compatibility into evidence your quality team can actually stand behind.

MR SAFETY & COMPATIBILITY EVALUATION

Seven Accredited MRI Safety Checkpoints

Part of our MRI Safety and Compatibility Testing for medical device panel, referenced to ASTM F2503

FDA MR safety guidance assessment on MRI scanner for medical device
01

FDA MR Safety Guidance Assessment

FDA MR Guidance

Magnetically induced displacement force test fixture in MRI bore for medical device
02

Magnetically Induced Displacement Test

ASTM F2052

MRI torque testing fixture in scanner bore for medical device
03

Magnetically Induced Torque Test

ASTM F2213

RF heating test with wired gel phantom in MRI scanner for medical device
04

RF Heating Test

ASTM F2182

Image artefact test gel phantom preparation for MRI compatibility of medical device
05

Image Artefact Test

ASTM F2119

MR safety labelling test demonstration on MRI table for medical device
06

MR Safety Labelling Test

ASTM F2503

FDA testing for MRI compatibility empty scan room for medical device
07

FDA Testing for MRI Compatibility

FDA MR Guidance

How Our MRI Safety Testing Process Works

Four steps, from sample intake to a validated report

1

Guidance Review

Device reviewed against ASTM F2503 and current FDA MR guidance before testing begins.

2

Force & Torque

Magnetically induced displacement and torque measured inside the scanner bore.

3

Heating & Imaging

RF heating and image artefact evaluated using calibrated gel phantoms.

4

Certified Report

Delivered digitally with a supported MR Safe/Conditional/Unsafe label, ready for submission.

Standards Behind Our Medical Device Testing

CHECKPOINT SCOPE STANDARD
FDA testing for medical deviceDesign review against current FDA MR guidanceFDA MR Guidance
RF heating testing for medical deviceTemperature rise under simulated RF scan exposureASTM F2182
Magnetically Induced Torque TestRotational force exerted by the static fieldASTM F2213
MR safety labelling testing for medical deviceFinal MR Safe/Conditional/Unsafe designationASTM F2503
VISIT OUR LABORATORY

Kiyo R&D Lab – Oragadam

Our MRI safety and compatibility testing suite is based at No.13, Srinivasa Perumal Street, Panapakkam, Serapanacheri, Greater Chennai, Tamil Nadu 601301.

Frequently Asked Questions

What does MRI Safety and Compatibility Testing for medical device cover? +

It covers seven checkpoints — FDA guidance review, displacement force, torque, RF heating, image artefact, safety labelling, and FDA compatibility testing — referenced to ASTM F2503 and current FDA MR guidance.

Why does FDA testing for medical device MR compatibility happen before physical testing starts? +

Reviewing the device design against current FDA MR guidance first ensures the displacement, torque, heating, and artefact tests that follow are scoped to exactly what a regulatory submission will need, rather than duplicating work later.

Why is this checkpoint considered a high-priority item for medical device implants? +

RF-induced heating around metal components is one of the most common real-world MR safety incidents, and a visual inspection or bench test at room temperature would never catch it, which is why this checkpoint uses a wired gel phantom under simulated scan conditions.

What does this checkpoint actually confirm on the final device label? +

It confirms the final MR Safe, MR Conditional, or MR Unsafe designation printed on the label is fully backed by the displacement, torque, heating, and artefact data collected during the rest of the programme, not assigned by assumption.

How do I get a quote for this testing? +

Call us at 90876 86986, message us on WhatsApp, or fill in the enquiry form below with your device and testing needs.

Book Your MRI Safety Testing Today

Talk to our Oragadam team about RF heating, labelling, or a full MRI Safety and Compatibility Testing for medical device study for your medical device testing programme.

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