Philips received a complaint on the dfm100 device indicating square wave is coming in ecg.There was no patient involvement.The fse evaluated the device on site.The fse conducted the thorough device check and discovered that the customer is currently using local ecg cables.In the event of any issues arising, it may become challenging to identify the root cause with these cables.The fse connected the defibrillator analyzer, impulse 7000dp, and verified that the ecg graph appears to be functioning correctly.However, if the customer encounters any recurring issues with the ecg graph, the fse recommended replacing the existing cable with a philips ecg cable.The system is currently in good working condition.The device remains at the customer site and no further evaluation is warranted at this time.The efficia dfm100 defibrillator, model# 866199, is substantially similar to the heartstart xl+ defibrillator (model # 861290) and will be reported in the united states under device model # 861290.
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