MAUDE manufacturer profile

MEDTRONIC CRYOCATH LP · QZI

MAUDE profile for Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation

Key facts

Manufacturer MEDTRONIC CRYOCATH LP
Manufacturer group MEDTRONIC CRYOCATH LP
Product code QZI
Product code name Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation

At a glance

  • 1,000+ MAUDE reports
  • 1–9 Death reports
  • 100–999 Injury reports
  • 100–999 Malfunction reports
  • 10–99 Problems flagged by Orca1 signal analytics
  • No Clinical Signs, Symptoms or Conditions, Material Deformation, Material Twisted/Bent, Adverse Event Without Identified Device or Use Problem, Material Integrity Problem, Detachment of Device or Device Component, Break, Pericardial Effusion 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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