Device typeTranstelephonic implantable pacemaker analysis system: An assembly of devices designed to analyse the performance of an implanted pacemaker based on electrocardiographic measurements that can be monitored transtelephonically. It typically includes a computer-based pacemaker analyser, a 12-lead electrocardiograph (ECG), and a transtelephonic receiver and/or transmitter. It provides data taken directly from the patient (e.g., ECG electrodes are applied to the patient and a test magnet is placed over the pacemaker to activate it) or a pacemaker programmer. Signals are sent to the receiver where pacemaker function information is displayed. This system may also include a database that collects and stores patient data.
FDA categoryDefibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D), Implantable cardioverter defibrillator (non-CRT), implantable pacemaker Pulse-generator, Implantable pulse generator, pacemaker (non-CRT), Leadless pacemaker, Pacemaker/icd/crt non-implanted components, Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P), Pulse generator, permanent, implantable, Pulse-generator, single chamber, sensor driven, implantable
Device ID05414734509732
Catalog numberMN5000
AvailabilityPrescription
MRI safetyLabeling does not contain MRI Safety Information