MR safety implant and/or foreign body assessment by trained clinical staff, including identification and verification of implant components from appropriate sources (eg, surgical reports, imaging reports, medical device databases, device vendors, review of prior imaging), analyzing current MR conditional status of individual components and systems, and consulting published professional guidance with written report; initial 15 minutes.
MR safety implant &/or foreign body assessment by trained clinical staff, incl identification & verification of implant components from appropriate sources; initial 15 minutes