MAUDE manufacturer profile

ST. JUDE MEDICAL · OAE

MAUDE profile for Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation

Key facts

Manufacturer ST. JUDE MEDICAL
Manufacturer group ST. JUDE MEDICAL
Product code OAE
Product code name Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation

At a glance

  • 1,000+ MAUDE reports
  • 10–99 Death reports
  • 1,000+ Injury reports
  • 100–999 Malfunction reports
  • 10–99 Problems flagged by Orca1 signal analytics
  • Adverse Event Without Identified Device or Use Problem, Cardiac Perforation, No Clinical Signs, Symptoms or Conditions, Optical Problem, Fracture, Patient Device Interaction Problem, Communication or Transmission Problem, No Consequences Or Impact To Patient 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

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