DKE German Commission for Electrical, Electronic & Information Technologies of DIN and VDE
Assessment of the safety of magnetic resonance imaging for patients with an active implantable medical device
Abstract
This document is applicable to implantable parts of active implantable medical devices (AIMDs) intended to 232 be used in patients who undergo a magnetic resonance scan in a 1,5 T (64 MHz) or 3 T (128 MHz), 233 whole body cylindrical MR system, using the fixed (integrated) whole body coil.
Begin
2026-04-09
Planned document number
DIN ISO 10974
Project number
02233786
Responsible national committee
DKE/GK 813 - Elektrische und mechanische Sicherheit in der radiologischen Technik