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#HEART MONITOR IMPLANT MANUALS#
See product manuals for details and troubleshooting instructions. Wireless accessories available for use with LINQ II may experience connectivity or performance issues. MRI scans should be performed only in a specified MR environment under specified conditions as described in the LINQ II MRI Technical Manual. Patients with the LINQ II ICM should avoid sources of diathermy, high sources of radiation, electrosurgical cautery, external defibrillation, lithotripsy, therapeutic ultrasound, and radiofrequency ablation to avoid electrical reset of the device, and/or inappropriate sensing as described in the medical procedure and EMI Warnings, Precautions, and Guidance Manual. However, the patient’s particular medical condition may dictate whether or not a subcutaneous, chronically inserted device can be tolerated. There are no known contraindications for the insertion of the LINQ II ICM or its accessories. The device has not been tested specifically for pediatric use. patients who experience transient symptoms such as dizziness, palpitation, syncope, and chest pain that may suggest a cardiac arrhythmia.patients with clinical syndromes or situations at increased risk of cardiac arrhythmias.
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The LINQ II ICM is an insertable automatically activated and patient-activated monitoring system that records subcutaneous ECG and is indicated in the following cases: Medtronic LINQ II Insertable Cardiac Monitor System (ICM) and Remote Monitoring For Cardiac Diagnostics & Monitoring Systems