MAUDE manufacturer profile

MPRI · OJX

MAUDE profile for Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode

Key facts

Manufacturer MPRI
Manufacturer group MPRI
Product code OJX
Product code name Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode

At a glance

  • 1,000+ MAUDE reports
  • 100–999 Death reports
  • 1,000+ Injury reports
  • 1,000+ Malfunction reports
  • 100–999 Problems flagged by Orca1 signal analytics
  • Adverse Event Without Identified Device or Use Problem, No Clinical Signs, Symptoms or Conditions, No Known Impact Or Consequence To Patient, High Capture Threshold, Unspecified Infection, Device Dislodged or Dislocated, Failure to Capture, Capturing Problem 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