According to current knowledge and guidelines of scientific societies, MRI in patients with an cardiac implantable electronic device are possible with respect to safety principles and should be considered and applied in selected clinical situations. The small number of centres performing these examinations means that patients in need of this type of diagnostics have limited access to it, which may affect the timing and selection of appropriate specialist treatment. This article discusses step by step the path of qualification and management of the implanted device, both approved for being in the electromagnetic field and without this certification, and presents the programming path for devices of different manufacturers, that are used in Poland – Abbott, Biotronik, Boston Scientific and Medtronic.