Information was received from a healthcare professional (hcp) via a manufacturer representative regarding a patient with an implantable neurostimulator (ins).It was reported that the patient went in to have their device interrogated and their impedance registered at 900; c-2 and c-3 was just over 400, but 2 & 3 was 900.It was noted that the battery was low and the patient needed a battery change to be scheduled.The issue was not resolved at the time of the report and surgical intervention was planned.No further complications were reported/anticipated.
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