MAUDE manufacturer profile

MEDTRONIC IRELAND · NIQ

MAUDE profile for Coronary Drug-Eluting Stent

Key facts

Manufacturer MEDTRONIC IRELAND
Manufacturer group MEDTRONIC IRELAND
Product code NIQ
Product code name Coronary Drug-Eluting Stent

At a glance

  • 1,000+ MAUDE reports
  • 1,000+ 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, Material Deformation, No Consequences Or Impact To Patient, No Clinical Signs, Symptoms or Conditions, Myocardial Infarction, Device Dislodged or Dislocated, Insufficient Information, Death 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