MAUDE manufacturer profile

MEDTRONIC NEUROMODULATION · DXY

MAUDE profile for Implantable Pacemaker Pulse-Generator

Key facts

Manufacturer MEDTRONIC NEUROMODULATION
Manufacturer group MEDTRONIC NEUROMODULATION
Product code DXY
Product code name Implantable Pacemaker Pulse-Generator

At a glance

  • 10–99 MAUDE reports
  • 1–9 Death reports
  • 10–99 Injury reports
  • 1–9 Malfunction reports
  • 10–99 Problems flagged by Orca1 signal analytics
  • No Clinical Signs, Symptoms or Conditions, Adverse Event Without Identified Device or Use Problem, Unspecified Infection, Signal Artifact/Noise, Over-Sensing, High impedance, Impedance Problem, Appropriate Term/Code Not Available Most reported problems

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About MAUDE manufacturer and product code profiles

Manufacturer profiles aggregate MAUDE reports for one manufacturer within one product code, the level at which device safety signals are usually reviewed.

Source: U.S. Food and Drug Administration (FDA), MAUDE database; aggregation by Orca1

Browse all MAUDE manufacturer and product code profiles