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Official Description

MR safety determination by a physician or other qualified health care professional responsible for the safety of the MR procedure, including review of implant MR conditions for indicated MR examination, analysis of risk vs clinical benefit of performing MR examination, and determination of MR equipment, accessory equipment, and expertise required to perform examination, with written report

© Copyright 2026 American Medical Association. All rights reserved.

Common Language Description

The CPT® Code 76016 pertains to the process of determining the safety of a magnetic resonance (MR) imaging procedure, specifically when a patient has an implanted medical device. This determination is conducted by a physician or another qualified healthcare professional who is responsible for ensuring the safety of the MR examination. The procedure involves a comprehensive review of the patient's implant MR conditions that are relevant to the indicated MR examination. The healthcare professional analyzes the potential risks versus the clinical benefits of performing the MR examination, taking into account the specific characteristics of the implanted device, such as pacemakers or neurostimulators, which may present contraindications or necessitate modifications to the examination protocol. Additionally, the safety determination includes an evaluation of incomplete or non-functioning devices that may not have clear safety condition labeling. The professional identifies the location and type of any foreign body present in the patient and reviews the details regarding the implant, including the manufacturer's labeling for any MRI restrictions or contraindications. The feasibility of the intended MRI exam is assessed based on these factors, along with the expected quality of the imaging that can be achieved while adhering to the implant's instructions and restrictions. Furthermore, the healthcare provider evaluates the potential risks to the patient, particularly by assessing the proximity of the implanted device to the target tissues and considering any risks of device malfunction, heat injury, or displacement during the MR examination. The report generated from this safety determination also outlines the requirements for any special accessory MR equipment needed and the expertise required to set up and conduct the examination safely. Recommendations for alternative diagnostic procedures may also be included, ensuring that all expectations, recommendations, and special precautions are communicated to the patient prior to finalizing the report.

© Copyright 2026 Coding Ahead. All rights reserved.

1. Indications

The MR safety determination is indicated in the following scenarios:

  • Implanted Medical Devices The procedure is necessary for patients who have implanted medical devices, such as pacemakers or neurostimulators, which may pose potential contraindications for an MR examination.
  • Incomplete or Non-Functioning Devices It is also indicated for patients with incomplete or non-functioning devices that may lack clear safety condition labeling, requiring a thorough evaluation before proceeding with an MR exam.

2. Procedure

The procedure for MR safety determination involves several critical steps to ensure patient safety during the MR examination:

  • Step 1: Identification of Foreign Bodies The healthcare professional begins by identifying the location and type of any foreign body present in the patient. This includes a detailed assessment of the implanted medical device, which is crucial for understanding the potential risks associated with the MR examination.
  • Step 2: Review of Implant Details Following the identification, the professional reviews the details regarding the implant, including the manufacturer's labeling for any MRI restrictions or contraindications. This step is essential to ascertain whether the device is compatible with the MR environment.
  • Step 3: Feasibility Analysis The next step involves analyzing the feasibility of the intended MRI exam based on the implant's instructions and restrictions. The healthcare provider evaluates the quality of imaging that can be expected while adhering to these guidelines.
  • Step 4: Risk Assessment A thorough risk assessment is conducted, focusing on the proximity of the implanted device to the target tissues. The provider considers potential risks such as device malfunction, heat injury, or displacement during the MR examination.
  • Step 5: Equipment and Expertise Requirements The report includes an outline of any special accessory MR equipment required for the examination, as well as the expertise necessary for setting up and conducting the MR exam safely.
  • Step 6: Recommendations and Precautions Finally, the healthcare professional provides recommendations for any alternative diagnostic procedures if necessary. All expectations, recommendations, and special precautions are communicated to the patient before finalizing the report.

3. Post-Procedure

After the MR safety determination is completed, the healthcare provider ensures that the patient is fully informed about the findings and any necessary precautions that must be taken during the MR examination. The written report detailing the safety assessment, including any recommendations for alternative procedures, is provided to the patient and relevant healthcare team members. It is crucial that the patient understands the implications of the findings, including any risks associated with the MR examination based on their specific medical device. Continuous communication and follow-up may be necessary to address any concerns or questions the patient may have regarding the procedure.

Short Descr MR SAFETY DETER PHYS/QHP
Medium Descr MR SAFETY DETERMINATION PHYSICIAN/OTHER QHP
Long Descr MR safety determination by a physician or other qualified health care professional responsible for the safety of the MR procedure, including review of implant MR conditions for indicated MR examination, analysis of risk vs clinical benefit of performing MR examination, and determination of MR equipment, accessory equipment, and expertise required to perform examination, with written report
Status Code Active Code
Global Days XXX - Global Concept Does Not Apply
PC/TC Indicator (26, TC) 1 - Diagnostic Tests for Radiology Services
Multiple Procedures (51) 4 - Special payment adjustment rules on the technical component (TC) of multiple diagnostic imaging procedures apply...
Bilateral Surgery (50) 0 - 150% payment adjustment for bilateral procedures does NOT apply.
Physician Supervisions 09 - Concept does not apply.
Assistant Surgeon (80, 82) 0 - Payment restriction for assistants at surgery applies to this procedure...
Co-Surgeons (62) 0 - Co-surgeons not permitted for this procedure.
Team Surgery (66) 0 - Team surgeons not permitted for this procedure.
Diagnostic Imaging Family 88 -
APC Status Indicator Procedure or Service, Not Discounted when Multiple
Type of Service (TOS) 4 - Diagnostic Radiology
Berenson-Eggers TOS (BETOS) none
MUE Not applicable/unspecified.
Date
Action
Notes
2025-01-01 Added Code Added.
Code
Description
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