MAUDE manufacturer profile

TERUMO CORPORATION, ASHITAKA · NIP

MAUDE profile for Stent, Superficial Femoral Artery

Key facts

Manufacturer TERUMO CORPORATION, ASHITAKA
Manufacturer group TERUMO CORPORATION, ASHITAKA
Product code NIP
Product code name Stent, Superficial Femoral Artery

At a glance

  • 100–999 MAUDE reports
  • 10–99 Injury reports
  • 10–99 Malfunction reports
  • 10–99 Problems flagged by Orca1 signal analytics
  • No Clinical Signs, Symptoms or Conditions, Material Deformation, Activation, Positioning or Separation Problem, No Consequences Or Impact To Patient, No Known Impact Or Consequence To Patient, Stretched, Activation Problem, Fracture 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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