Recorder, event, implantable cardiac, (without arrhythmia detection)

FDA product code MXC · Class 2 · 5 devices · 2,430 reports · 2 deaths reported · 0 devices named in recalls

• Assert-IQ™ DM5500

  St. Jude Medical, Inc. · Recorder, event, implantable cardiac, (without arrhythmia detection)
  951 reports
• Assert-IQ™ DM5300

  St. Jude Medical, Inc. · Recorder, event, implantable cardiac, (without arrhythmia detection)
  949 reports
• SJM CONFIRM™ DM2102

  St. Jude Medical, Inc. · RECORDER,EVENT,IMPLANTABLE CARDIAC,(WITHOUT ARRHYTHMIA DETECTION)
  251 reports
• Assert-IQ™ DM5000

  St. Jude Medical, Inc. · Recorder, event, implantable cardiac, (without arrhythmia detection)
  226 reports
• SJM CONFIRM™ DM2100

  St. Jude Medical, Inc. · RECORDER,EVENT,IMPLANTABLE CARDIAC,(WITHOUT ARRHYTHMIA DETECTION)
  2 deaths53 reports